The post is for a doctor who is interested in pursuing the Portfolio route with the support of the department. The department is very busy and receives approximately 250 suspected skin cancer referrals per week. Tele dermatology is well established and outpatient rooms, procedure rooms, and a UV suite are collocated in Rowan House. Main duties of the job The main duties of the post include outpatient clinics for both adults and paediatric patients, minor surgery, and ward cover for urgent referrals. The successful applicant will be responsible for the delivery and development of high-quality dermatology care under the supervision of the consultant team. About us We are a people business where every member of staff matters and can make a difference. Patients are at the heart of everything we do. Joining University Hospitals Plymouth NHS Trust means becoming part of a team of dedicated staff, who are committed to leading the way through innovation, clinical excellence, and great customer care. The Trust has great opportunities for career development in a highly progressive working environment. We offer all of this in a vibrant, modern city with a historic reputation for adventure. PLEASE NOTE THAT ALL COMMUNICATION WILL BE ELECTRONIC, PLEASE CHECK YOUR EMAIL ACCOUNT REGULARLY. If you have any issues with applying online and need additional support including reasonable adjustments with the application process, please contact the recruitment team on . We recognise that work-life balance is important for our colleagues and so we invite requests from applicants around less than full-time/flexible working for our advertised roles. Please contact the recruiting manager to discuss this prior to your application submission. We commit to giving this full consideration in each case. We encourage people from diverse backgrounds to apply for our roles, as diversity strengthens our teams. It is sometimes necessary to close vacancies before the closing date. If you have not heard from us within 4 weeks of the closing date, please assume that you have not been shortlisted. Job responsibilities The post holder will also be expected to participate in the normal duties relating to the administration of the Dermatology Department. These duties will include teaching, continuing medical education, and audit/clinical governance. Person Specification Qualifications MBBS or equivalent & Postgraduate MRCP (UK) or (I). Non-UK graduates without MRCP must provide evidence of appropriate knowledge, training, and experience, particularly in the case of acute medical conditions. Experience A sound knowledge of basic clinical sciences and the ability to apply this knowledge to clinical practice. An understanding of dermatology and relevant clinical experience including outpatient working. Understanding of principles of audit, research, and evidence-based medicine. Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Feb 06, 2025
Full time
The post is for a doctor who is interested in pursuing the Portfolio route with the support of the department. The department is very busy and receives approximately 250 suspected skin cancer referrals per week. Tele dermatology is well established and outpatient rooms, procedure rooms, and a UV suite are collocated in Rowan House. Main duties of the job The main duties of the post include outpatient clinics for both adults and paediatric patients, minor surgery, and ward cover for urgent referrals. The successful applicant will be responsible for the delivery and development of high-quality dermatology care under the supervision of the consultant team. About us We are a people business where every member of staff matters and can make a difference. Patients are at the heart of everything we do. Joining University Hospitals Plymouth NHS Trust means becoming part of a team of dedicated staff, who are committed to leading the way through innovation, clinical excellence, and great customer care. The Trust has great opportunities for career development in a highly progressive working environment. We offer all of this in a vibrant, modern city with a historic reputation for adventure. PLEASE NOTE THAT ALL COMMUNICATION WILL BE ELECTRONIC, PLEASE CHECK YOUR EMAIL ACCOUNT REGULARLY. If you have any issues with applying online and need additional support including reasonable adjustments with the application process, please contact the recruitment team on . We recognise that work-life balance is important for our colleagues and so we invite requests from applicants around less than full-time/flexible working for our advertised roles. Please contact the recruiting manager to discuss this prior to your application submission. We commit to giving this full consideration in each case. We encourage people from diverse backgrounds to apply for our roles, as diversity strengthens our teams. It is sometimes necessary to close vacancies before the closing date. If you have not heard from us within 4 weeks of the closing date, please assume that you have not been shortlisted. Job responsibilities The post holder will also be expected to participate in the normal duties relating to the administration of the Dermatology Department. These duties will include teaching, continuing medical education, and audit/clinical governance. Person Specification Qualifications MBBS or equivalent & Postgraduate MRCP (UK) or (I). Non-UK graduates without MRCP must provide evidence of appropriate knowledge, training, and experience, particularly in the case of acute medical conditions. Experience A sound knowledge of basic clinical sciences and the ability to apply this knowledge to clinical practice. An understanding of dermatology and relevant clinical experience including outpatient working. Understanding of principles of audit, research, and evidence-based medicine. Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Product Manager (Software) - Cambridge - Hybrid working model - 50k to 60k This is a fantastic opportunity for someone with an Engineering or Computer Science/Programming background, keen to join a dynamic Product team working on a range of high-performing RF products! This role has a strong focus on product documentation, so candidates will need to demonstrate strong technical capability/accumen. What will you be doing? Become the voice of customer - sourcing, compiling and analysing the market (including competitor information) Aid in the ownership of the Product lifecycle Work with the software team to prioritise sprints and track tickets in JIRA Ensure all products meet customer requirements and are positioned within the market effectively What soft skills can I bring? Positive attitude and a willingness to learn Ability to develop strong relationships Understand technical concepts to collaborate with the wider team and stakeholders What can my background look like? Graduate level degree in Computer Science or Engineering Experience with signal processing/ wireless comms or RF systems Software development/programming experience (flexibility on language/framework) Experience with embedded platforms What are the benefits? Genuine opportunities for career progression and professional development Flexible working hours Remote working 2 days a week Health insurance Pension 25 days holiday plus bank holidays
Feb 06, 2025
Full time
Product Manager (Software) - Cambridge - Hybrid working model - 50k to 60k This is a fantastic opportunity for someone with an Engineering or Computer Science/Programming background, keen to join a dynamic Product team working on a range of high-performing RF products! This role has a strong focus on product documentation, so candidates will need to demonstrate strong technical capability/accumen. What will you be doing? Become the voice of customer - sourcing, compiling and analysing the market (including competitor information) Aid in the ownership of the Product lifecycle Work with the software team to prioritise sprints and track tickets in JIRA Ensure all products meet customer requirements and are positioned within the market effectively What soft skills can I bring? Positive attitude and a willingness to learn Ability to develop strong relationships Understand technical concepts to collaborate with the wider team and stakeholders What can my background look like? Graduate level degree in Computer Science or Engineering Experience with signal processing/ wireless comms or RF systems Software development/programming experience (flexibility on language/framework) Experience with embedded platforms What are the benefits? Genuine opportunities for career progression and professional development Flexible working hours Remote working 2 days a week Health insurance Pension 25 days holiday plus bank holidays
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management. A fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics . Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). Responsibilities Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy Compile and maintain project-specific status reports within the clinical trial management system Interact with the internal project team, Sponsor, study sites, and third-party vendors Provide oversight and quality control of our internal regulatory filing system Provide oversight and management of study supplies Create and maintain project timelines Coordinate project meetings and produce quality minutes Qualifications PhD in Life Sciences Fluency in English with solid presentation skills Ability to work in a fast-paced dynamic industry within an international team Prior experience within the CRO or pharmaceutical industry not required but will be advantageous Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets
Feb 06, 2025
Full time
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management. A fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics . Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). Responsibilities Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy Compile and maintain project-specific status reports within the clinical trial management system Interact with the internal project team, Sponsor, study sites, and third-party vendors Provide oversight and quality control of our internal regulatory filing system Provide oversight and management of study supplies Create and maintain project timelines Coordinate project meetings and produce quality minutes Qualifications PhD in Life Sciences Fluency in English with solid presentation skills Ability to work in a fast-paced dynamic industry within an international team Prior experience within the CRO or pharmaceutical industry not required but will be advantageous Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management. A fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics . Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). Responsibilities Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy Compile and maintain project-specific status reports within the clinical trial management system Interact with the internal project team, Sponsor, study sites, and third-party vendors Provide oversight and quality control of our internal regulatory filing system Provide oversight and management of study supplies Create and maintain project timelines Coordinate project meetings and produce quality minutes Qualifications PhD in Life Sciences Fluency in English with solid presentation skills Ability to work in a fast-paced dynamic industry within an international team Prior experience within the CRO or pharmaceutical industry not required but will be advantageous Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets
Feb 06, 2025
Full time
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management. A fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics . Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). Responsibilities Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy Compile and maintain project-specific status reports within the clinical trial management system Interact with the internal project team, Sponsor, study sites, and third-party vendors Provide oversight and quality control of our internal regulatory filing system Provide oversight and management of study supplies Create and maintain project timelines Coordinate project meetings and produce quality minutes Qualifications PhD in Life Sciences Fluency in English with solid presentation skills Ability to work in a fast-paced dynamic industry within an international team Prior experience within the CRO or pharmaceutical industry not required but will be advantageous Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets
Medpace is currently seeking candidates with Renal related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our London Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management. A fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics . Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). Responsibilities Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy Compile and maintain project-specific status reports within the clinical trial management system Interact with the internal project team, Sponsor, study sites, and third-party vendors Provide oversight and quality control of our internal regulatory filing system Provide oversight and management of study supplies Create and maintain project timelines Coordinate project meetings and produce quality minutes Qualifications PhD in Life Sciences Fluency in English with solid presentation skills Ability to work in a fast-paced dynamic industry within an international team Prior experience within the CRO or pharmaceutical industry not required but will be advantageous Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets
Feb 06, 2025
Full time
Medpace is currently seeking candidates with Renal related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our London Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management. A fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics . Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). Responsibilities Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy Compile and maintain project-specific status reports within the clinical trial management system Interact with the internal project team, Sponsor, study sites, and third-party vendors Provide oversight and quality control of our internal regulatory filing system Provide oversight and management of study supplies Create and maintain project timelines Coordinate project meetings and produce quality minutes Qualifications PhD in Life Sciences Fluency in English with solid presentation skills Ability to work in a fast-paced dynamic industry within an international team Prior experience within the CRO or pharmaceutical industry not required but will be advantageous Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets
Contract: Permanent Hours: Full time (37.5 hours) Salary: £25,000 - £26,000 per annum Location: Gloucester, Hybrid working for 2 days per week at home Closing date: 4th March 2025 We will review applications and conduct interviews as they are received and therefore this post may be filled before the closing date if a suitable candidate is found. For this reason, we advise early applications. Our client is looking for an enthusiastic, organized, and efficient Academic Coordinator to join their friendly team. In this essential role, you'll coordinate the daily operations of their accredited education programs, ensuring smooth delivery and excellent service to their students and tutors. If you're passionate about supporting postgraduate education, skilled in communication, and enjoy working as part of a team, they would love to hear from you. Our client offers a comprehensive range of Continuing Professional Development (CPD) courses for veterinary surgeons and nurses. As the Academic Coordinator, you'll play a vital role in organizing, supporting, and resourcing the Association's postgraduate programs to ensure their success. You will join a dedicated operational team of five within their wider Continuing Education department In this diverse role, you will handle a range of responsibilities including managing student inquiries and enrolment, administering committees, and coordinating the delivery of their accredited programs. This involves liaising with students, speakers, supervisors, and mentors, as well as working with venue and equipment providers. You'll also assist in organizing formal examinations, hosting online lectures and webinars, and maintaining their learning platform. Skills and experience: They're seeking a well-organised professional who can manage multiple tasks with precision. Strong communication skills, a collaborative approach, and the ability to prioritise and meet deadlines are essential for success in this role. They're looking for a candidate with a strong background in administrative support within a fast-paced environment. Experience in coordinating, delivering, and hosting professional training events, or in maintaining academic records, is desirable. Familiarity with educational platforms and technology is a plus, though not required, as training will be provided. You must be flexible to occasionally work outside of normal office hours to facilitate delivery of their courses. Other essential skills include: - Proficiency in Microsoft Office and general IT skills - A proactive, self-motivated approach to handling tasks - A flexible approach to work - Willingness to learn Our client is a professional membership association which exists to advance care for companion animals. With a membership of more than 10,000 veterinary surgeons, vet nurses and students, they work in the UK and internationally to promote excellence in small animal practice through education and science, by facilitating training, conducting research, and developing policy. Each year they deliver numerous education courses, host a large, small-animal Congress, and publish books, manuals, apps, and magazines. This post sits within the Education department and reports to the Academic Operations Manager. Their reward package for this role includes a basic salary of between £25,000 - £26,000 per annum (depending on experience). In addition, they offer generous employer pension contributions starting at 7% and increasing up to 10% with length of service. They also offer: - Holiday starting at 25 days (plus bank holidays) rising by 1 day each year up to 28 days, plus a further entitlement of an additional one day every 5 years of service. - Bupa dental plan. - Enhanced pay for maternity, paternity, adoption and other family-related leave. - Life assurance of 3 x annual salary. - Support for hybrid working for their employees, meaning you can work at home for two days per week, and they also have a comprehensive Flexible Working Policy. - Access to a free legal helpline where you can ask their specialist lawyers for legal advice on an array of topics. - Health and wellbeing support available 24/7 365 days and a network of mental health first aiders. Plus, enhanced Company sick pay, access to private medical insurance upon completion of 12 months' service, occupational health service and annual flu vaccinations. - Training and development. - Free onsite parking, and for those who wish to cycle, they offer a cycle to work scheme which provides a discounted purchase of a bicycle and accessories for healthy, low carbon travel. And they are: Committed to supporting sustainability in their work and in the veterinary profession. The Association has completed a certified carbon audit and has been awarded silver accreditation with Investors in the Environment. So, if you are bold and innovative, strive for excellence whilst taking ownership and accountability of your work, show passion for what you do and work effectively in a team - then you'll be a great fit for the Association, and they would love to hear from you. How to apply: In order to be considered for this role, please submit your CV and a cover letter detailing how you meet the requirements in the role description which is on their vacancy page. Their commitment to equality, diversity and inclusion (EDI) underpins their belief that they can make the Association stronger through the unique contributions they can all bring. They create inclusive teams aligned to their values and encourage applications from a diverse range of suitably qualified candidates. You may also have experience in the following roles: Education Coordinator, Learning and Development Coordinator, Training Administrator, Programme Coordinator, Academic Administrator, Student Support Officer, CPD Coordinator, Events Coordinator, Training Support Officer, Membership Coordinator, or similar positions, etc. REF-
Feb 05, 2025
Full time
Contract: Permanent Hours: Full time (37.5 hours) Salary: £25,000 - £26,000 per annum Location: Gloucester, Hybrid working for 2 days per week at home Closing date: 4th March 2025 We will review applications and conduct interviews as they are received and therefore this post may be filled before the closing date if a suitable candidate is found. For this reason, we advise early applications. Our client is looking for an enthusiastic, organized, and efficient Academic Coordinator to join their friendly team. In this essential role, you'll coordinate the daily operations of their accredited education programs, ensuring smooth delivery and excellent service to their students and tutors. If you're passionate about supporting postgraduate education, skilled in communication, and enjoy working as part of a team, they would love to hear from you. Our client offers a comprehensive range of Continuing Professional Development (CPD) courses for veterinary surgeons and nurses. As the Academic Coordinator, you'll play a vital role in organizing, supporting, and resourcing the Association's postgraduate programs to ensure their success. You will join a dedicated operational team of five within their wider Continuing Education department In this diverse role, you will handle a range of responsibilities including managing student inquiries and enrolment, administering committees, and coordinating the delivery of their accredited programs. This involves liaising with students, speakers, supervisors, and mentors, as well as working with venue and equipment providers. You'll also assist in organizing formal examinations, hosting online lectures and webinars, and maintaining their learning platform. Skills and experience: They're seeking a well-organised professional who can manage multiple tasks with precision. Strong communication skills, a collaborative approach, and the ability to prioritise and meet deadlines are essential for success in this role. They're looking for a candidate with a strong background in administrative support within a fast-paced environment. Experience in coordinating, delivering, and hosting professional training events, or in maintaining academic records, is desirable. Familiarity with educational platforms and technology is a plus, though not required, as training will be provided. You must be flexible to occasionally work outside of normal office hours to facilitate delivery of their courses. Other essential skills include: - Proficiency in Microsoft Office and general IT skills - A proactive, self-motivated approach to handling tasks - A flexible approach to work - Willingness to learn Our client is a professional membership association which exists to advance care for companion animals. With a membership of more than 10,000 veterinary surgeons, vet nurses and students, they work in the UK and internationally to promote excellence in small animal practice through education and science, by facilitating training, conducting research, and developing policy. Each year they deliver numerous education courses, host a large, small-animal Congress, and publish books, manuals, apps, and magazines. This post sits within the Education department and reports to the Academic Operations Manager. Their reward package for this role includes a basic salary of between £25,000 - £26,000 per annum (depending on experience). In addition, they offer generous employer pension contributions starting at 7% and increasing up to 10% with length of service. They also offer: - Holiday starting at 25 days (plus bank holidays) rising by 1 day each year up to 28 days, plus a further entitlement of an additional one day every 5 years of service. - Bupa dental plan. - Enhanced pay for maternity, paternity, adoption and other family-related leave. - Life assurance of 3 x annual salary. - Support for hybrid working for their employees, meaning you can work at home for two days per week, and they also have a comprehensive Flexible Working Policy. - Access to a free legal helpline where you can ask their specialist lawyers for legal advice on an array of topics. - Health and wellbeing support available 24/7 365 days and a network of mental health first aiders. Plus, enhanced Company sick pay, access to private medical insurance upon completion of 12 months' service, occupational health service and annual flu vaccinations. - Training and development. - Free onsite parking, and for those who wish to cycle, they offer a cycle to work scheme which provides a discounted purchase of a bicycle and accessories for healthy, low carbon travel. And they are: Committed to supporting sustainability in their work and in the veterinary profession. The Association has completed a certified carbon audit and has been awarded silver accreditation with Investors in the Environment. So, if you are bold and innovative, strive for excellence whilst taking ownership and accountability of your work, show passion for what you do and work effectively in a team - then you'll be a great fit for the Association, and they would love to hear from you. How to apply: In order to be considered for this role, please submit your CV and a cover letter detailing how you meet the requirements in the role description which is on their vacancy page. Their commitment to equality, diversity and inclusion (EDI) underpins their belief that they can make the Association stronger through the unique contributions they can all bring. They create inclusive teams aligned to their values and encourage applications from a diverse range of suitably qualified candidates. You may also have experience in the following roles: Education Coordinator, Learning and Development Coordinator, Training Administrator, Programme Coordinator, Academic Administrator, Student Support Officer, CPD Coordinator, Events Coordinator, Training Support Officer, Membership Coordinator, or similar positions, etc. REF-
Medpace is currently seeking candidates with Cardiovascular related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our London Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management. A fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics . Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). Responsibilities Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy Compile and maintain project-specific status reports within the clinical trial management system Interact with the internal project team, Sponsor, study sites, and third-party vendors Provide oversight and quality control of our internal regulatory filing system Provide oversight and management of study supplies Create and maintain project timelines Coordinate project meetings and produce quality minutes Qualifications PhD in Life Sciences Fluency in English with solid presentation skills Ability to work in a fast-paced dynamic industry within an international team Prior experience within the CRO or pharmaceutical industry not required but will be advantageous Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets
Feb 05, 2025
Full time
Medpace is currently seeking candidates with Cardiovascular related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our London Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management. A fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics . Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). Responsibilities Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy Compile and maintain project-specific status reports within the clinical trial management system Interact with the internal project team, Sponsor, study sites, and third-party vendors Provide oversight and quality control of our internal regulatory filing system Provide oversight and management of study supplies Create and maintain project timelines Coordinate project meetings and produce quality minutes Qualifications PhD in Life Sciences Fluency in English with solid presentation skills Ability to work in a fast-paced dynamic industry within an international team Prior experience within the CRO or pharmaceutical industry not required but will be advantageous Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets
NES Fircroft are working with a well-renowned Crop Protection Soultions company, who are looking for a Scientific Technologist to offer cross-functional support to their Particle Science and Process Engineering Teams. A great opportunity, ideal for recent graduates, this position offers a unique chance to learn from experts in the scientific and engineering fields, opening doors to a range of career paths. This is an initial 24 Month Contract Opportunity This role is crucial in order to improve and develop manufacturing processes for new and existing products via technical understanding to support manufacturing plants and projects in meeting business targets. Skills - Should have experience of laboratory operations (Ideally 1-2 years) - Experience with any of the following analytical techniques would be beneficial: DSC, TGA, XRD, SEM, NMR, HPLC and GC. - Experience with powder handling, crystalisations and wet chemistry would be beneficial Education - Degree in chemistry, chemical or process engineering Don't miss out on this opportunity! Contact us today for more details With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider spanning the Oil & Gas, Power & Renewables, Chemicals, Construction & Infrastructure, Life Sciences, Mining and Manufacturing sectors worldwide. With more than 80 offices in 45 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. We offer contractors far more than a traditional recruitment service, supporting with everything from securing visas and work permits, to providing market-leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.
Feb 05, 2025
Contractor
NES Fircroft are working with a well-renowned Crop Protection Soultions company, who are looking for a Scientific Technologist to offer cross-functional support to their Particle Science and Process Engineering Teams. A great opportunity, ideal for recent graduates, this position offers a unique chance to learn from experts in the scientific and engineering fields, opening doors to a range of career paths. This is an initial 24 Month Contract Opportunity This role is crucial in order to improve and develop manufacturing processes for new and existing products via technical understanding to support manufacturing plants and projects in meeting business targets. Skills - Should have experience of laboratory operations (Ideally 1-2 years) - Experience with any of the following analytical techniques would be beneficial: DSC, TGA, XRD, SEM, NMR, HPLC and GC. - Experience with powder handling, crystalisations and wet chemistry would be beneficial Education - Degree in chemistry, chemical or process engineering Don't miss out on this opportunity! Contact us today for more details With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider spanning the Oil & Gas, Power & Renewables, Chemicals, Construction & Infrastructure, Life Sciences, Mining and Manufacturing sectors worldwide. With more than 80 offices in 45 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. We offer contractors far more than a traditional recruitment service, supporting with everything from securing visas and work permits, to providing market-leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.
About the role Strategy and Communications Strategy and Communications sits at the centre of the organisation, bringing together several teams with organisation-wide remits and mutual collaboration opportunities. The work of the directorate's teams includes delivery of major events, designing and leading public affairs or marketing campaigns, providing data, evidence and analysis, leading cross-organisational programmes, to making sure we plan for and can respond to emerging events or emergencies in our city. About the team The City Data Team is made up of a range of technical experts in the fields of Data Science and Engineering, Data Visualisation and Information Design, GIS and Mapping, and Demographic Modelling and Analysis. The team sits alongside economist and social policy analysts within City Intelligence - a central unit of City Hall serving the Mayor, the London Assembly, the Greater London Authority (GLA) and London. Our chief purpose is to provide world-class evidence, analysis and tools for the Mayor and his team to formulate outcomes, strategies, policies and delivery plans in London - and to help with their delivery. We aim to communicate an up-to-date understanding of London, its communities, its economy and its place in a rapidly changing wider world. We work with others to innovate and develop evidence-based policies, programmes and projects that will make a positive difference to London and Londoners. About the role The GLA produces a range of demographic projections to meet the needs of planners and policy makers across London. These projections are used to help deliver local services, identify future infrastructure needs, and form a key part of the evidence base for London's Spatial Development Strategy. The core purpose of the role is to contribute to the ongoing development of the models and systems used to produce and deliver the projections, to ensure the best possible information is available to underpin decisions about housing, transport, education, and infrastructure, that affect the lives of millions of people. You will be working on the team's current priorities for the models: Restructuring and refactoring our existing (R) codebase to simplify the process of updating models and producing outputs. Developing improvements to existing methodologies used to estimate and project individual components of population change and account for alternative assumptions about future housing deliver, jobs growth, and transport infrastructure. Performing analysis of retrospective projections to better understand the strengths and weaknesses of our existing models. Improving how we capture and communicate uncertainty in the projections. What your day will look like Stand-up call with the team to update on progress and flag issues. Research and assess potential methods for use in the projections, producing a short technical note of your findings for review by the team. Coordinate with colleagues who are working to update our data infrastructure and identify changes to existing model code necessary to adapt. Call with users to discuss their requirements and receive feedback on existing outputs. Contribute to a code or methodology review requested by a colleague in a neighbouring team. Skills, knowledge and experience To be considered for the role you must meet the following essential criteria: A high level of numeracy and technical knowledge, typically evidenced by a graduate qualification in statistics, mathematics, or an allied subject or exceptionally, by at least five years' experience in a similar role. Professional experience working with R and/or Python, and the use of version control systems for collaborative development. Able to appropriately select and apply a wide range of modelling and analytical techniques to real world problems. Experience in undertaking project-based work - adapting to deadlines and producing clear documentation of code and assumptions. Able to communicate complex technical ideas to a range of audiences. Job Purpose To contribute to the development and maintenance of the GLA's suite of demographic models and analytical tools, leading on the publication of outputs, technical notes, and related analysis as required. To work with stakeholders in the GLA, functional bodies and London Boroughs, providing analytical support and ensuring that their intelligence needs are met. To provide expert advice and support on the development and use of models across the wider organisation, promoting best practice in the application of statistics and data science. To help deliver the team's programme of analysis and reporting and to develop new and innovative demographic modelling and analytical products to support the needs of policy makers in service provision and future planning for London. Principal accountabilities Contribute to the ongoing maintenance, quality assurance, and improvement of the Demography Team's suite of models. To work with a wide range of internal and external stakeholders to identify requirements and to address these by providing appropriate analysis, modelling, and expert guidance. To deliver projections and analytical outputs as part the range of data services provided by the team to internal and external users. To ensure outputs are produced to high professional standards and are accompanied by appropriate guidance and information to allow stakeholders to correctly interpret and apply the results. To engage with and share expertise with stakeholders, providing support and guidance, and promoting best practice in the application of data science and modelling. To undertake analysis and evaluation of alternative data sources, models, and methods, to help guide the team's technical decisions. To realise the benefits of working in an open and collaborative manner, ensuring that models and analysis are reproducible and appropriately documented, being transparent with results and methods, and encouraging engagement with the team's work. To realise the benefits of London's diversity by promoting and enabling equality of opportunities and promoting the diverse needs and aspirations of London's communities. Realise the benefits of a flexible approach to work in undertaking the duties and responsibilities of this job, and participating in multi-disciplinary, cross-department projects. Manage staff and resources in allocated to the job in accordance with the Authority's policies and Code of Ethics and Standards Person specification Technical requirements/experience/qualifications A high level of numeracy and technical knowledge, evidenced by a graduate qualification in information technology, information systems, statistics, applied mathematics, or an allied subject or exceptionally, by at least five years' experience in a similar role. Professional experience working with R and/or Python, and the use of version control systems for collaborative development. Able to appropriately select and apply a wide range of modelling and analytical techniques to real world problems. Spatial analysis skills and experience in working with large, complex datasets. Evidence of success in undertaking project-based work, designing and preparing clear and concise reports, presentations and briefings on complex issues. Evidence of success in building and forming working relationships, and working flexibly, across professional and operational boundaries within an organisation, and with external organisations. An understanding of the GLA's commitment to equality of opportunity and valuing diversity, and the ability to translate this into action. Research and Analysis is gathering intelligence (information, opinion and data) from varied sources, making sense of it, testing its validity and drawing conclusions that can lead to practical benefits. Level 3 indicators of effective performance Expands networks to gain new information sources for research and policy development Identifies and implements methods to ensure intelligence is of a high quality Encourages others to analyse data from different angles, using multiple perspectives to identify connections and new insights Tailors research investment in line with likely impact for Londoners and policy priorities Retains a bigger picture view, ensuring research recommendations are appropriate and practical for the GLA and its stakeholders Stakeholder Focus is consulting with, listening to and understanding the needs of those our work impacts and using this knowledge to shape what we do and manage others' expectations. Level 3 indicators of effective performance Understands diverse stakeholder needs and tailors team deliverables accordingly Is a role model to others, encouraging them to think of Londoners first Manages stakeholder expectations, so they are high but realistic Removes barriers to understanding the needs of diverse stakeholders, including hard to reach groups Focuses own and team's efforts on delivering a quality and committed service Communicating and Influencing is presenting information and arguments clearly and convincingly so that others see us as credible and articulate, and engage with us. Level 3 indicators of effective performance . click apply for full job details
Feb 05, 2025
Full time
About the role Strategy and Communications Strategy and Communications sits at the centre of the organisation, bringing together several teams with organisation-wide remits and mutual collaboration opportunities. The work of the directorate's teams includes delivery of major events, designing and leading public affairs or marketing campaigns, providing data, evidence and analysis, leading cross-organisational programmes, to making sure we plan for and can respond to emerging events or emergencies in our city. About the team The City Data Team is made up of a range of technical experts in the fields of Data Science and Engineering, Data Visualisation and Information Design, GIS and Mapping, and Demographic Modelling and Analysis. The team sits alongside economist and social policy analysts within City Intelligence - a central unit of City Hall serving the Mayor, the London Assembly, the Greater London Authority (GLA) and London. Our chief purpose is to provide world-class evidence, analysis and tools for the Mayor and his team to formulate outcomes, strategies, policies and delivery plans in London - and to help with their delivery. We aim to communicate an up-to-date understanding of London, its communities, its economy and its place in a rapidly changing wider world. We work with others to innovate and develop evidence-based policies, programmes and projects that will make a positive difference to London and Londoners. About the role The GLA produces a range of demographic projections to meet the needs of planners and policy makers across London. These projections are used to help deliver local services, identify future infrastructure needs, and form a key part of the evidence base for London's Spatial Development Strategy. The core purpose of the role is to contribute to the ongoing development of the models and systems used to produce and deliver the projections, to ensure the best possible information is available to underpin decisions about housing, transport, education, and infrastructure, that affect the lives of millions of people. You will be working on the team's current priorities for the models: Restructuring and refactoring our existing (R) codebase to simplify the process of updating models and producing outputs. Developing improvements to existing methodologies used to estimate and project individual components of population change and account for alternative assumptions about future housing deliver, jobs growth, and transport infrastructure. Performing analysis of retrospective projections to better understand the strengths and weaknesses of our existing models. Improving how we capture and communicate uncertainty in the projections. What your day will look like Stand-up call with the team to update on progress and flag issues. Research and assess potential methods for use in the projections, producing a short technical note of your findings for review by the team. Coordinate with colleagues who are working to update our data infrastructure and identify changes to existing model code necessary to adapt. Call with users to discuss their requirements and receive feedback on existing outputs. Contribute to a code or methodology review requested by a colleague in a neighbouring team. Skills, knowledge and experience To be considered for the role you must meet the following essential criteria: A high level of numeracy and technical knowledge, typically evidenced by a graduate qualification in statistics, mathematics, or an allied subject or exceptionally, by at least five years' experience in a similar role. Professional experience working with R and/or Python, and the use of version control systems for collaborative development. Able to appropriately select and apply a wide range of modelling and analytical techniques to real world problems. Experience in undertaking project-based work - adapting to deadlines and producing clear documentation of code and assumptions. Able to communicate complex technical ideas to a range of audiences. Job Purpose To contribute to the development and maintenance of the GLA's suite of demographic models and analytical tools, leading on the publication of outputs, technical notes, and related analysis as required. To work with stakeholders in the GLA, functional bodies and London Boroughs, providing analytical support and ensuring that their intelligence needs are met. To provide expert advice and support on the development and use of models across the wider organisation, promoting best practice in the application of statistics and data science. To help deliver the team's programme of analysis and reporting and to develop new and innovative demographic modelling and analytical products to support the needs of policy makers in service provision and future planning for London. Principal accountabilities Contribute to the ongoing maintenance, quality assurance, and improvement of the Demography Team's suite of models. To work with a wide range of internal and external stakeholders to identify requirements and to address these by providing appropriate analysis, modelling, and expert guidance. To deliver projections and analytical outputs as part the range of data services provided by the team to internal and external users. To ensure outputs are produced to high professional standards and are accompanied by appropriate guidance and information to allow stakeholders to correctly interpret and apply the results. To engage with and share expertise with stakeholders, providing support and guidance, and promoting best practice in the application of data science and modelling. To undertake analysis and evaluation of alternative data sources, models, and methods, to help guide the team's technical decisions. To realise the benefits of working in an open and collaborative manner, ensuring that models and analysis are reproducible and appropriately documented, being transparent with results and methods, and encouraging engagement with the team's work. To realise the benefits of London's diversity by promoting and enabling equality of opportunities and promoting the diverse needs and aspirations of London's communities. Realise the benefits of a flexible approach to work in undertaking the duties and responsibilities of this job, and participating in multi-disciplinary, cross-department projects. Manage staff and resources in allocated to the job in accordance with the Authority's policies and Code of Ethics and Standards Person specification Technical requirements/experience/qualifications A high level of numeracy and technical knowledge, evidenced by a graduate qualification in information technology, information systems, statistics, applied mathematics, or an allied subject or exceptionally, by at least five years' experience in a similar role. Professional experience working with R and/or Python, and the use of version control systems for collaborative development. Able to appropriately select and apply a wide range of modelling and analytical techniques to real world problems. Spatial analysis skills and experience in working with large, complex datasets. Evidence of success in undertaking project-based work, designing and preparing clear and concise reports, presentations and briefings on complex issues. Evidence of success in building and forming working relationships, and working flexibly, across professional and operational boundaries within an organisation, and with external organisations. An understanding of the GLA's commitment to equality of opportunity and valuing diversity, and the ability to translate this into action. Research and Analysis is gathering intelligence (information, opinion and data) from varied sources, making sense of it, testing its validity and drawing conclusions that can lead to practical benefits. Level 3 indicators of effective performance Expands networks to gain new information sources for research and policy development Identifies and implements methods to ensure intelligence is of a high quality Encourages others to analyse data from different angles, using multiple perspectives to identify connections and new insights Tailors research investment in line with likely impact for Londoners and policy priorities Retains a bigger picture view, ensuring research recommendations are appropriate and practical for the GLA and its stakeholders Stakeholder Focus is consulting with, listening to and understanding the needs of those our work impacts and using this knowledge to shape what we do and manage others' expectations. Level 3 indicators of effective performance Understands diverse stakeholder needs and tailors team deliverables accordingly Is a role model to others, encouraging them to think of Londoners first Manages stakeholder expectations, so they are high but realistic Removes barriers to understanding the needs of diverse stakeholders, including hard to reach groups Focuses own and team's efforts on delivering a quality and committed service Communicating and Influencing is presenting information and arguments clearly and convincingly so that others see us as credible and articulate, and engage with us. Level 3 indicators of effective performance . click apply for full job details
Graduate/Junior Software Engineer required by a small but well-established software company based in central Reading. The company develop analytical web applications used by the emergency services and are currently looking for another Graduate/Junior to join their existing development team of 4. The role will be focused on developing simulation-based applications, therefore any exposure to simulation or numerical computing would preferred. The core programming language of the company is C#, however this is something they are happy to provide training on. They also will work with other languages depending on requirements including SQL, C++, Python, and NodeJS. The company are happy to consider someone who has already graduated and looking for a new role, or someone who is due to graduate in 2025. Experience in the following is required: Degree in Computer Science or other numerate subject such as Mathematics or Physics Mathematics A level at grade A or B. Knowledge of a mainstream programming language such as: C#, Java, C++, Python During the 3-month probation period this would be an office-based role however following successful completion, the company operate on a hybrid model involving typically 50% of time in the office. The company also currently trialling a 9 day fortnight, so every other Friday is a day off! This is a great opportunity to join a really interesting cutting-edge software company working on applications that have a real-life impact. If you are interested in this position, please contact (url removed) or call (phone number removed). Spectrum IT Recruitment (South) Limited is acting as an Employment Agency in relation to this vacancy.
Feb 05, 2025
Full time
Graduate/Junior Software Engineer required by a small but well-established software company based in central Reading. The company develop analytical web applications used by the emergency services and are currently looking for another Graduate/Junior to join their existing development team of 4. The role will be focused on developing simulation-based applications, therefore any exposure to simulation or numerical computing would preferred. The core programming language of the company is C#, however this is something they are happy to provide training on. They also will work with other languages depending on requirements including SQL, C++, Python, and NodeJS. The company are happy to consider someone who has already graduated and looking for a new role, or someone who is due to graduate in 2025. Experience in the following is required: Degree in Computer Science or other numerate subject such as Mathematics or Physics Mathematics A level at grade A or B. Knowledge of a mainstream programming language such as: C#, Java, C++, Python During the 3-month probation period this would be an office-based role however following successful completion, the company operate on a hybrid model involving typically 50% of time in the office. The company also currently trialling a 9 day fortnight, so every other Friday is a day off! This is a great opportunity to join a really interesting cutting-edge software company working on applications that have a real-life impact. If you are interested in this position, please contact (url removed) or call (phone number removed). Spectrum IT Recruitment (South) Limited is acting as an Employment Agency in relation to this vacancy.
Graduate Sports Betting Analyst, Computer Science, Physics, Maths, Engineering, Russell Group, London, Sports Graduate Sports Betting Analyst About Us We are currently working with a market-leading Sports Betting company that works across all sports in the betting industry. The role The role will be primary focused on working with a wide range of sports and clients, understanding and analysing their needs and assessing odds. Our client is looking to take on a confident candidate who is equally comfortable mathematically and in sporting knowledge. You will be workering as Sports Betting Analyst so you must have good knowledge of Sports and Statistics. There is fast progression with this position for motivated applicants. A strong interest in betting and sports is essential along with a high aptitude for numeracy. Responsibilities . Analyst data in line with client requirements. Build rapport with a wide range of clients. Communicating regularly with major stakeholders. Assist in odd creation Organisation with great timekeeping. Qualifications 2:1 or above BSc in a technical or numerate discipline (Maths, Physics, Computer Science or Engineering) from Russel Group University. Strong communication skills and a will to succeed. Must have exceptional kmnowledge of sports Must have full UK working rights. Salary: £36,000+ Full-time, Permanent Other benefits: Opportunity to become share holder Gym membership Generous pension scheme Graduate Sports Betting Analyst, Computer Science, Physics, Maths, Engineering, Russell Group, London, Sports
Feb 05, 2025
Full time
Graduate Sports Betting Analyst, Computer Science, Physics, Maths, Engineering, Russell Group, London, Sports Graduate Sports Betting Analyst About Us We are currently working with a market-leading Sports Betting company that works across all sports in the betting industry. The role The role will be primary focused on working with a wide range of sports and clients, understanding and analysing their needs and assessing odds. Our client is looking to take on a confident candidate who is equally comfortable mathematically and in sporting knowledge. You will be workering as Sports Betting Analyst so you must have good knowledge of Sports and Statistics. There is fast progression with this position for motivated applicants. A strong interest in betting and sports is essential along with a high aptitude for numeracy. Responsibilities . Analyst data in line with client requirements. Build rapport with a wide range of clients. Communicating regularly with major stakeholders. Assist in odd creation Organisation with great timekeeping. Qualifications 2:1 or above BSc in a technical or numerate discipline (Maths, Physics, Computer Science or Engineering) from Russel Group University. Strong communication skills and a will to succeed. Must have exceptional kmnowledge of sports Must have full UK working rights. Salary: £36,000+ Full-time, Permanent Other benefits: Opportunity to become share holder Gym membership Generous pension scheme Graduate Sports Betting Analyst, Computer Science, Physics, Maths, Engineering, Russell Group, London, Sports
Graduate IT Recruitment Consultant - Southampton, Hampshire - 24k- 26k + Commission Graduate IT Recruitment Consultant required to join Southampton's leading IT Recruitment Company. Spectrum IT Recruitment was established 15 years ago and has gained significant market share since we started. We are looking for a talented graduate who is keen to pursue a career in IT Recruitment / Sales and who wants to be rewarded for their hard work. The ideal candidate will ideally have some sales experience and a sense of strong customer service. If you don't have any sales experience, do still apply if you can show a strong background in customer service. This is a fantastic environment for a graduate who has the desire to make money and be rewarded for it. We offer an excellent commission scheme ensuring that you get rewarded for the placements you make. You will work alongside and learn from some of the best recruiters in the business. We recently took all the consultants who hit their target last year to Dubai for an all-expenses-paid trip. As well as yearly trips abroad, there are quarterly incentives plus nights out and early finishes. Spectrum IT Recruitment is based on the Southampton Science Park which offers free parking, an onsite cafe, Best Western Chilworth Manor Hotel and Leisure Club. No car or maybe you don't drive. No problem - There is also a dedicated bus which services multiple transport routes to and from the Science Park. Interested? Send your CV for immediate consideration to (url removed) or call (phone number removed) for more details. Spectrum IT Recruitment (South) Limited is acting as an Employment Agency in relation to this vacancy.
Feb 05, 2025
Full time
Graduate IT Recruitment Consultant - Southampton, Hampshire - 24k- 26k + Commission Graduate IT Recruitment Consultant required to join Southampton's leading IT Recruitment Company. Spectrum IT Recruitment was established 15 years ago and has gained significant market share since we started. We are looking for a talented graduate who is keen to pursue a career in IT Recruitment / Sales and who wants to be rewarded for their hard work. The ideal candidate will ideally have some sales experience and a sense of strong customer service. If you don't have any sales experience, do still apply if you can show a strong background in customer service. This is a fantastic environment for a graduate who has the desire to make money and be rewarded for it. We offer an excellent commission scheme ensuring that you get rewarded for the placements you make. You will work alongside and learn from some of the best recruiters in the business. We recently took all the consultants who hit their target last year to Dubai for an all-expenses-paid trip. As well as yearly trips abroad, there are quarterly incentives plus nights out and early finishes. Spectrum IT Recruitment is based on the Southampton Science Park which offers free parking, an onsite cafe, Best Western Chilworth Manor Hotel and Leisure Club. No car or maybe you don't drive. No problem - There is also a dedicated bus which services multiple transport routes to and from the Science Park. Interested? Send your CV for immediate consideration to (url removed) or call (phone number removed) for more details. Spectrum IT Recruitment (South) Limited is acting as an Employment Agency in relation to this vacancy.
Science Teacher / Science ECT In the heart of Westminster an 'Outstanding' Secondary School are on the hunt for a Science Teacher / Science ECT for a September 2025 start. This is a permanent, and full-time contract. The Head Teacher is looking for an ambitious Science Teacher / Science ECT who is keen to add value to an expanding Science Department. The school is renowned for their supportive SLT, and impressive Progress 8 results across all subjects. Why would you want to work at this remarkable School? Head Teacher is a natural leader, works with staff, not against them. When she left her previous School, the following year - 66% of staff left. Feeder School for two high achieving Sixth Forms KS3-5 2,000 Bonus (Per Year) Moving away from the standard "death by PP" (Good questioning & modeling is a must) Abundance of additional support for pupils (to benefit staff) Huge TLR opportunities Good work life balance! Modern marking policy (you don't take any work home) Can leave work at 3:30pm! & much much more! Experienced Science Teachers can take on a TLR such as KS3 Coordinator, Pastoral Responsibility and more. Newly Qualified Science Teachers (NQT) will be enrolled onto the schools very own bespoke ECT induction, as well as work alongside a range of young & experienced Science Teachers. Does this sound like the Science Teacher / Science ECT for you? If so, please read on below to find out further information! JOB DESCRIPTION Science Teacher / Science ECT Inspiring and motivating the younger generation Working alongside a team of fantastic Science Teachers TLR Opportunities: KS3 Coordinator and Pastoral Responsibilities ECTs welcome: 1:1 Mentor, bespoke ECT induction, In & out of house training and more September 2025 - Full Time & Permanent MPS1-UPS3 - 39,571 - 65,000 + TLR (Size depending on experience) Located in the Borough of Westminster PERSON SPECIFICATION Must have UK QTS or be in the process of gaining Strong academics across the board - Degree, A Levels and GCSEs Must be meeting the 8 Teaching Standards to a 'Good or Outstanding' level You must be able to work as part of a large team of Science Teachers Must be willing to listen to feedback SCHOOL DETAILS Graded 'Outstanding' in latest Ofsted report Impressive Progress 8 results Modern & creative facilities throughout Impeccable behavior throughout the School Plenty of additional support in class from graduate Teaching Assistants Good Tube Links - Westminster Carpark onsite If you are interested in this Science Teacher / Science ECT opportunity , interviews & lesson observations can be arranged immediately Apply for this Science Teacher / Science ECT opportunity by sending your CV to Ryan at EdEx. You will be contacted by your personal consultant (if shortlisted)! Science Teacher / Science ECT
Feb 05, 2025
Full time
Science Teacher / Science ECT In the heart of Westminster an 'Outstanding' Secondary School are on the hunt for a Science Teacher / Science ECT for a September 2025 start. This is a permanent, and full-time contract. The Head Teacher is looking for an ambitious Science Teacher / Science ECT who is keen to add value to an expanding Science Department. The school is renowned for their supportive SLT, and impressive Progress 8 results across all subjects. Why would you want to work at this remarkable School? Head Teacher is a natural leader, works with staff, not against them. When she left her previous School, the following year - 66% of staff left. Feeder School for two high achieving Sixth Forms KS3-5 2,000 Bonus (Per Year) Moving away from the standard "death by PP" (Good questioning & modeling is a must) Abundance of additional support for pupils (to benefit staff) Huge TLR opportunities Good work life balance! Modern marking policy (you don't take any work home) Can leave work at 3:30pm! & much much more! Experienced Science Teachers can take on a TLR such as KS3 Coordinator, Pastoral Responsibility and more. Newly Qualified Science Teachers (NQT) will be enrolled onto the schools very own bespoke ECT induction, as well as work alongside a range of young & experienced Science Teachers. Does this sound like the Science Teacher / Science ECT for you? If so, please read on below to find out further information! JOB DESCRIPTION Science Teacher / Science ECT Inspiring and motivating the younger generation Working alongside a team of fantastic Science Teachers TLR Opportunities: KS3 Coordinator and Pastoral Responsibilities ECTs welcome: 1:1 Mentor, bespoke ECT induction, In & out of house training and more September 2025 - Full Time & Permanent MPS1-UPS3 - 39,571 - 65,000 + TLR (Size depending on experience) Located in the Borough of Westminster PERSON SPECIFICATION Must have UK QTS or be in the process of gaining Strong academics across the board - Degree, A Levels and GCSEs Must be meeting the 8 Teaching Standards to a 'Good or Outstanding' level You must be able to work as part of a large team of Science Teachers Must be willing to listen to feedback SCHOOL DETAILS Graded 'Outstanding' in latest Ofsted report Impressive Progress 8 results Modern & creative facilities throughout Impeccable behavior throughout the School Plenty of additional support in class from graduate Teaching Assistants Good Tube Links - Westminster Carpark onsite If you are interested in this Science Teacher / Science ECT opportunity , interviews & lesson observations can be arranged immediately Apply for this Science Teacher / Science ECT opportunity by sending your CV to Ryan at EdEx. You will be contacted by your personal consultant (if shortlisted)! Science Teacher / Science ECT
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in nuclear medicine, medical physics, medical imaging / radiopharmaceuticals or / radiation oncology for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management. A fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge radiopharmaceuticals (molecular radiotherapy, radiotheranostics, targeted radionuclide therapy) . Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). Responsibilities Communicate and collaborate on global study activities; working closely with the Project Coordinator and Clinical Trial Manager Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy Compile and maintain project-specific status reports within the clinical trial management system Interact with the internal project team, Sponsor, study sites, and third-party vendors Provide oversight and quality control of our internal regulatory filing system Provide oversight and management of study supplies Create and maintain project timelines Coordinate project meetings and produce quality minutes Qualifications PhD or Post-Doc related to Radiopharmaceuticals ( nuclear medicine/medical physics/medical imaging/ radiation oncology or related ) Fluency in English with solid presentation skills Ability to work in a fast-paced dynamic industry within an international team Prior experience within the CRO or pharmaceutical industry not required but will be advantageous Medpace Overview Medpace is a full-service clinical contract research organisation (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets
Feb 05, 2025
Full time
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in nuclear medicine, medical physics, medical imaging / radiopharmaceuticals or / radiation oncology for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management. A fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge radiopharmaceuticals (molecular radiotherapy, radiotheranostics, targeted radionuclide therapy) . Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). Responsibilities Communicate and collaborate on global study activities; working closely with the Project Coordinator and Clinical Trial Manager Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy Compile and maintain project-specific status reports within the clinical trial management system Interact with the internal project team, Sponsor, study sites, and third-party vendors Provide oversight and quality control of our internal regulatory filing system Provide oversight and management of study supplies Create and maintain project timelines Coordinate project meetings and produce quality minutes Qualifications PhD or Post-Doc related to Radiopharmaceuticals ( nuclear medicine/medical physics/medical imaging/ radiation oncology or related ) Fluency in English with solid presentation skills Ability to work in a fast-paced dynamic industry within an international team Prior experience within the CRO or pharmaceutical industry not required but will be advantageous Medpace Overview Medpace is a full-service clinical contract research organisation (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets
Pharmaceutical Account Manager - Primary Care - Dorset & East Devon Our client is a major leading Pharmaceutical Organisation dedicated to improve the quality of human life. We are currently looking for "Best in Class" sales professionals to join them in achieving their mission. You will be a respiratory therapy and disease expert working across a specific geography within primary care, responsible and accountable for the customers and the performance of that geography. You will be excited to play a pivotal role in the larger Area Therapy team to ensure the optimum use of resources and flow of customer and competitor information. You must be comfortable being held accountable for the performance of a territory. Intellectually nimble and capable of keeping knowledge levels high across disease, you will have to be an expert on your own products, competitors, and local environment. Able to work on your own initiative and a self-starter, you have a hunger for self-development and a desire to be seen as the best in class when it comes to selling and influencing skills. Ideally, you will have a proven track record of achievement in sales from a similar role in the UK pharmaceutical industry and a life science degree. We are also keen to hear from graduate calibre candidates with previous sales experience from a different sector, seeking their first Pharmaceutical role. A Highly Competitive Basic Salary, Company Car, Benefits Package and Bonus will be offered. To discuss this position please apply online or contact CHASE for further information on . Reference Number: 60971
Feb 05, 2025
Full time
Pharmaceutical Account Manager - Primary Care - Dorset & East Devon Our client is a major leading Pharmaceutical Organisation dedicated to improve the quality of human life. We are currently looking for "Best in Class" sales professionals to join them in achieving their mission. You will be a respiratory therapy and disease expert working across a specific geography within primary care, responsible and accountable for the customers and the performance of that geography. You will be excited to play a pivotal role in the larger Area Therapy team to ensure the optimum use of resources and flow of customer and competitor information. You must be comfortable being held accountable for the performance of a territory. Intellectually nimble and capable of keeping knowledge levels high across disease, you will have to be an expert on your own products, competitors, and local environment. Able to work on your own initiative and a self-starter, you have a hunger for self-development and a desire to be seen as the best in class when it comes to selling and influencing skills. Ideally, you will have a proven track record of achievement in sales from a similar role in the UK pharmaceutical industry and a life science degree. We are also keen to hear from graduate calibre candidates with previous sales experience from a different sector, seeking their first Pharmaceutical role. A Highly Competitive Basic Salary, Company Car, Benefits Package and Bonus will be offered. To discuss this position please apply online or contact CHASE for further information on . Reference Number: 60971
The successful candidate will be responsible for testing and analysing materials, products, and processes to ensure the quality and performance of automotive glass. This role requires a solid understanding of materials science, attention to detail, and proficiency with lab equipment and safety protocols. Client Details The client is a leading manufacturer and supplier of high-performance automotive glass, specialising in the production of advanced glass solutions for vehicles in Europe. Description We are looking for a hands-on Lab Technician to join a leading automotive glass manufacturer. This is an exciting opportunity to play a crucial role in testing and manufacturing high-performance automotive glass components. As a Lab Technician, you will be involved in a variety of tasks, including sample measuring, preparation, and testing using advanced equipment such as environmental test chambers, QUV's QSUNS, and drop ball rigs. Sample measuring and preparation for testing Conducting environmental tests and using QUV's QSUNS and pellet impact tests Operating clean room equipment for manufacturing and testing parts Writing detailed reports on test findings and analysis Maintaining and ensuring proper functioning of lab equipment Coordinating with service engineers for equipment servicing and troubleshooting Assisting project managers and providing support across testing and manufacturing tasks Profile Background in materials, chemistry, or physics (biology/pharmaceutical experience not applicable) Experience in quality control and testing Practical, hands-on approach to testing and manufacturing Strong communication skills for reporting and assisting project managers No degree required, but NVQ, HND, or work-based qualifications are preferred Mid-career professionals or Open University graduates are welcome, but recent graduates may also be considered Job Offer (phone number removed) with room for negotiation based on experience Flexible working hours and a balanced work-life environment Opportunity for career development in a dynamic industry Annual Bonus Pension
Feb 05, 2025
Full time
The successful candidate will be responsible for testing and analysing materials, products, and processes to ensure the quality and performance of automotive glass. This role requires a solid understanding of materials science, attention to detail, and proficiency with lab equipment and safety protocols. Client Details The client is a leading manufacturer and supplier of high-performance automotive glass, specialising in the production of advanced glass solutions for vehicles in Europe. Description We are looking for a hands-on Lab Technician to join a leading automotive glass manufacturer. This is an exciting opportunity to play a crucial role in testing and manufacturing high-performance automotive glass components. As a Lab Technician, you will be involved in a variety of tasks, including sample measuring, preparation, and testing using advanced equipment such as environmental test chambers, QUV's QSUNS, and drop ball rigs. Sample measuring and preparation for testing Conducting environmental tests and using QUV's QSUNS and pellet impact tests Operating clean room equipment for manufacturing and testing parts Writing detailed reports on test findings and analysis Maintaining and ensuring proper functioning of lab equipment Coordinating with service engineers for equipment servicing and troubleshooting Assisting project managers and providing support across testing and manufacturing tasks Profile Background in materials, chemistry, or physics (biology/pharmaceutical experience not applicable) Experience in quality control and testing Practical, hands-on approach to testing and manufacturing Strong communication skills for reporting and assisting project managers No degree required, but NVQ, HND, or work-based qualifications are preferred Mid-career professionals or Open University graduates are welcome, but recent graduates may also be considered Job Offer (phone number removed) with room for negotiation based on experience Flexible working hours and a balanced work-life environment Opportunity for career development in a dynamic industry Annual Bonus Pension
Physics Data Scientist Closing Date: 4th March 2025 Location: RG7 4PR , located between Reading and Basingstoke, with free onsite parking . Due to the classified nature of the work involved, the successful candidate will spend the majority of their time on site at AWE Aldermaston. Occasional working from home is quite normal for those in this role but there will need to be flexibility around working pattern to meet business requirements. Package: £28,420-£39,500 (depending on your suitability, qualifications, and level of experience) Working pattern: AWE operates a 9-day working fortnight. We will consider flexible working requests so that your work may fit in with your lifestyle. Just let us know your preferred working pattern on your application. Let us introduce the role AWE is currently recruiting for a Data Scientist within the Systems Assessment Group focused on the Nuclear Threat Reduction mission space . This role is ideally suited to a physicist with a keen focus on Data Science who enjoys working with diverse teams on a wide area including Radiation Detection, Computational Modelling and Machine Learning . Working with extant teams of subject matter experts from a variety of backgrounds the successful candidate will both apply and develop their Data Science skills by addressing real world problems pertaining to nuclear threat reduction. In addition to Nuclear Threat Reduction project work the successful candidate will help provide decision making support for the business through data science analysis and modelling; working in a team of specialists to provide information and insights using their applied data science knowledge. They will further contribute to the future of AWE by understanding and optimising data science processes, analysis and experimental design using appropriate libraries, software and tools developing a deep understanding of the nuclear defence sector. Who are we looking for? We do need you to have the following: A strong degree in Physics or a related subject with a focus on applied science. Postgraduate degrees such as MPhys, MSc, MEng, and PhD would also be welcome. Ability to develop code in languages like R, Python, MATLAB, C++, FORTRAN. Whilst not to be considered a tick list, we'd like you to have experience in some of the following: Experience working with scientific/engineering/academic teams focusing on data science and an understanding of data science best practice. The ability to convey complex and highly technical issues to diverse audiences. Familiarity with common libraries for statistical analysis, data assessment and machine learning and the software development lifecycle. A structured approach to problem solving. You'll need to have the ability to work calmly and constructively in a priority changing environment and be able to manage your own workload. You will also have initiative, enthusiasm, a flexible approach, and ability to work to tight deadlines. Some reasons we think you'll love it here: AWE has wide range of benefits to suit you. These include: 9-day working fortnight - meaning you get every other Friday off work, in addition to 270 hours of annual leave. Market leading contributory pension scheme (we will pay between 9% and 13% of your pensionable pay depending on your contributions). Family friendly policies: Maternity Leave - 39 Weeks Full Pay and Paternity Leave - 4 Weeks Full Pay. Opportunities for Professional Career Development including funding for annual membership of a relevant professional body. Employee Assistance Programme and Occupational Health Services. Life Assurance (4 x annual salary). Discounts - access to savings on a wide range of everyday spending. Special Leave Policy including paid time off for volunteering, public service (including reserve forces) and caring. The 'Working at AWE' page on our website is where you can find full details in the 'AWE Benefits Guide'.
Feb 04, 2025
Full time
Physics Data Scientist Closing Date: 4th March 2025 Location: RG7 4PR , located between Reading and Basingstoke, with free onsite parking . Due to the classified nature of the work involved, the successful candidate will spend the majority of their time on site at AWE Aldermaston. Occasional working from home is quite normal for those in this role but there will need to be flexibility around working pattern to meet business requirements. Package: £28,420-£39,500 (depending on your suitability, qualifications, and level of experience) Working pattern: AWE operates a 9-day working fortnight. We will consider flexible working requests so that your work may fit in with your lifestyle. Just let us know your preferred working pattern on your application. Let us introduce the role AWE is currently recruiting for a Data Scientist within the Systems Assessment Group focused on the Nuclear Threat Reduction mission space . This role is ideally suited to a physicist with a keen focus on Data Science who enjoys working with diverse teams on a wide area including Radiation Detection, Computational Modelling and Machine Learning . Working with extant teams of subject matter experts from a variety of backgrounds the successful candidate will both apply and develop their Data Science skills by addressing real world problems pertaining to nuclear threat reduction. In addition to Nuclear Threat Reduction project work the successful candidate will help provide decision making support for the business through data science analysis and modelling; working in a team of specialists to provide information and insights using their applied data science knowledge. They will further contribute to the future of AWE by understanding and optimising data science processes, analysis and experimental design using appropriate libraries, software and tools developing a deep understanding of the nuclear defence sector. Who are we looking for? We do need you to have the following: A strong degree in Physics or a related subject with a focus on applied science. Postgraduate degrees such as MPhys, MSc, MEng, and PhD would also be welcome. Ability to develop code in languages like R, Python, MATLAB, C++, FORTRAN. Whilst not to be considered a tick list, we'd like you to have experience in some of the following: Experience working with scientific/engineering/academic teams focusing on data science and an understanding of data science best practice. The ability to convey complex and highly technical issues to diverse audiences. Familiarity with common libraries for statistical analysis, data assessment and machine learning and the software development lifecycle. A structured approach to problem solving. You'll need to have the ability to work calmly and constructively in a priority changing environment and be able to manage your own workload. You will also have initiative, enthusiasm, a flexible approach, and ability to work to tight deadlines. Some reasons we think you'll love it here: AWE has wide range of benefits to suit you. These include: 9-day working fortnight - meaning you get every other Friday off work, in addition to 270 hours of annual leave. Market leading contributory pension scheme (we will pay between 9% and 13% of your pensionable pay depending on your contributions). Family friendly policies: Maternity Leave - 39 Weeks Full Pay and Paternity Leave - 4 Weeks Full Pay. Opportunities for Professional Career Development including funding for annual membership of a relevant professional body. Employee Assistance Programme and Occupational Health Services. Life Assurance (4 x annual salary). Discounts - access to savings on a wide range of everyday spending. Special Leave Policy including paid time off for volunteering, public service (including reserve forces) and caring. The 'Working at AWE' page on our website is where you can find full details in the 'AWE Benefits Guide'.
Graduate Client Product Success Manager Are you a recent graduate with a passion for technology and a drive for client satisfaction? We have an amazing opportunity for you! Our client, a leading software house and pioneer in artificial intelligence, is seeking a Graduate Client Product Success Manager to join their exceptional team. With their cutting-edge technology, they are revolutionising household organisations across the UK and beyond. In this role, you will collaborate with support and operations teams, ensuring a smooth onboarding process for clients. You will have the opportunity to travel both nationally and overseas, tailoring solutions to meet clients' needs. With a strong focus on client satisfaction, you will enjoy solving challenges and building rapport. To be successful in this role, you will need a 2.1 or higher in physics, natural sciences, biology, chemistry, history, or a related field from a leading university. Strong A-level grades are desired, as well as excellent written and verbal communication skills. While experience in a technology or software company is a plus, it is not essential. Our client's entrepreneurial management team, along with their team of brilliant academics and engineers, will provide a supportive and dynamic environment. With a hybrid working model, you will have the flexibility to thrive in a fast-paced, ever-changing organisation. If you're eager to start your career with a top AI company and make a real impact, don't miss out on this exciting opportunity. Apply now by clicking the link below. Please note that Adecco is operating as an Employment Agency. We are an equal opportunities employer, and your application will be handled with the utmost confidentiality. Rest assured, we will always reach out to you before sharing your CV with any potential employer.
Feb 04, 2025
Full time
Graduate Client Product Success Manager Are you a recent graduate with a passion for technology and a drive for client satisfaction? We have an amazing opportunity for you! Our client, a leading software house and pioneer in artificial intelligence, is seeking a Graduate Client Product Success Manager to join their exceptional team. With their cutting-edge technology, they are revolutionising household organisations across the UK and beyond. In this role, you will collaborate with support and operations teams, ensuring a smooth onboarding process for clients. You will have the opportunity to travel both nationally and overseas, tailoring solutions to meet clients' needs. With a strong focus on client satisfaction, you will enjoy solving challenges and building rapport. To be successful in this role, you will need a 2.1 or higher in physics, natural sciences, biology, chemistry, history, or a related field from a leading university. Strong A-level grades are desired, as well as excellent written and verbal communication skills. While experience in a technology or software company is a plus, it is not essential. Our client's entrepreneurial management team, along with their team of brilliant academics and engineers, will provide a supportive and dynamic environment. With a hybrid working model, you will have the flexibility to thrive in a fast-paced, ever-changing organisation. If you're eager to start your career with a top AI company and make a real impact, don't miss out on this exciting opportunity. Apply now by clicking the link below. Please note that Adecco is operating as an Employment Agency. We are an equal opportunities employer, and your application will be handled with the utmost confidentiality. Rest assured, we will always reach out to you before sharing your CV with any potential employer.
We are currently working with a major consultancy as they look to add a Senior Civil Engineer to their division in the City of London. With the team growing, this Senior Engineer position will provide you the opportunity to work in various sectors as part of an enthusiastic and committed team of engineers and technicians, where you will help develop the infrastructure capability of a growing Civil and Structural department. About You Relevant Degree and Chartered CIHT, ICE, IHE etc or working towards chartership Extensive experience of Autodesk Civil 3D, Microdrainage and AutoCAD A thorough understanding of earthworks design, below ground foul and surface water drainage design, pavement design, external works and 3D underground services co-ordination is required. You will have experience working in a multi-disciplinary team where you are able to take initiative and work independently, and be happy to mentor graduate and junior engineers Full UK drivers licence Why this Opportunity? You will work on exciting projects with niche clients in a range of sectors, including Life Sciences, Industrial, Custodial and Education You will join a team that value innovative ideas, client service and following best industry practice You will have access to the company's wider network of engineers where you can share ideas, discuss challenges and learn Potential for growth into leadership of the civil and structural team, you will be supported in achieving these goals though various learning opportunities as well as mentorship from the wider management team Company benefits include a generous company car or cash allowance, 6% matched pension contribution, flexible working, family friendly policies, an employee assistance programme, as well as a bonus scheme and paid professional subscriptions. This is a unique opportunity that is not to be missed. If you think your experience matches up well, please click apply or reach out to Jamie Will at Calibre Search. Calibre Search promote equality in the workplace and we welcome applications from all suitably skilled or qualified candidates regardless of their sex, race, disability, religion/beliefs, sexual orientation or age. We act as both an employment agency and employment business.
Feb 04, 2025
Full time
We are currently working with a major consultancy as they look to add a Senior Civil Engineer to their division in the City of London. With the team growing, this Senior Engineer position will provide you the opportunity to work in various sectors as part of an enthusiastic and committed team of engineers and technicians, where you will help develop the infrastructure capability of a growing Civil and Structural department. About You Relevant Degree and Chartered CIHT, ICE, IHE etc or working towards chartership Extensive experience of Autodesk Civil 3D, Microdrainage and AutoCAD A thorough understanding of earthworks design, below ground foul and surface water drainage design, pavement design, external works and 3D underground services co-ordination is required. You will have experience working in a multi-disciplinary team where you are able to take initiative and work independently, and be happy to mentor graduate and junior engineers Full UK drivers licence Why this Opportunity? You will work on exciting projects with niche clients in a range of sectors, including Life Sciences, Industrial, Custodial and Education You will join a team that value innovative ideas, client service and following best industry practice You will have access to the company's wider network of engineers where you can share ideas, discuss challenges and learn Potential for growth into leadership of the civil and structural team, you will be supported in achieving these goals though various learning opportunities as well as mentorship from the wider management team Company benefits include a generous company car or cash allowance, 6% matched pension contribution, flexible working, family friendly policies, an employee assistance programme, as well as a bonus scheme and paid professional subscriptions. This is a unique opportunity that is not to be missed. If you think your experience matches up well, please click apply or reach out to Jamie Will at Calibre Search. Calibre Search promote equality in the workplace and we welcome applications from all suitably skilled or qualified candidates regardless of their sex, race, disability, religion/beliefs, sexual orientation or age. We act as both an employment agency and employment business.
Compliance & Sustainability Assistant Fresh People are currently recruiting for a Compliance & Sustainability Assistant on behalf of our Fresh produce client based in the Maidstone area . In this role you will be focusing on technical compliance and sustainability administration and reporting. This role is integral to supporting our clients commitment to operating responsibly. Managing suppliers across various products and geographies to ensure food safety, ethical due diligence, and environmental monitoring The Person The ideal candidate will be educated with a degree preferably in Food Science , Environmental Management or Science would look at graduates , proficient in Microsoft Office Suite particularly Excel and Power BI . You will be required to work collaboratively with stakeholders across all levels , with a strong attention to detail and deadline focused. Key Responsibilities Liaise with suppliers to collate accurate and review due diligence information and file the records on internal and customer due diligence platforms. Monitor and report on due diligence throughout the supply period. Manage the daily chemical surveillance testing schedule for supplier arrivals. • Perform supplier recall and traceability exercises. Maintain and update approved supplier lists (Internal and customers) Collate, review and trend supplier environmental data relating to Food waste, Carbon Emissions, Water and Sustainable Farming certification. If you have the experience we require for this role then reach out today to discuss in more detail .
Feb 04, 2025
Full time
Compliance & Sustainability Assistant Fresh People are currently recruiting for a Compliance & Sustainability Assistant on behalf of our Fresh produce client based in the Maidstone area . In this role you will be focusing on technical compliance and sustainability administration and reporting. This role is integral to supporting our clients commitment to operating responsibly. Managing suppliers across various products and geographies to ensure food safety, ethical due diligence, and environmental monitoring The Person The ideal candidate will be educated with a degree preferably in Food Science , Environmental Management or Science would look at graduates , proficient in Microsoft Office Suite particularly Excel and Power BI . You will be required to work collaboratively with stakeholders across all levels , with a strong attention to detail and deadline focused. Key Responsibilities Liaise with suppliers to collate accurate and review due diligence information and file the records on internal and customer due diligence platforms. Monitor and report on due diligence throughout the supply period. Manage the daily chemical surveillance testing schedule for supplier arrivals. • Perform supplier recall and traceability exercises. Maintain and update approved supplier lists (Internal and customers) Collate, review and trend supplier environmental data relating to Food waste, Carbon Emissions, Water and Sustainable Farming certification. If you have the experience we require for this role then reach out today to discuss in more detail .