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PLEASE SUBMIT ENGLISH LANGUAGE RESUMES ONLY *Various Seniority Levels * Home-Based/Remote Based Contract Opportunity *Full Time (FTE 1.0) *6+ month duration Do you prefer flexible work options that allow you to work as a contractor, while also being immersed in the PPD Culture? Apply today to learn more about current and upcoming contractor opportunities through our Functional Service Partnership team. Functional Service Partnership Homepage: Position Summary Provides innovative solutions including regulatory expertise and client interface to provide strategic intelligence, and guidance supporting product development from preclinical through registration and product optimization. Provides strategic, expedient and efficient preparation of client deliverables that meet current local, regional and ICH regulatory and technical requirements. Acts as liaison with internal and external clients in the provision and marketing of these services. *Qualifications:* Essential Functions * Supports the preparation of documentation and submissions under guidance. * Coordinates and manages client deliverables supporting regulatory compliance. * Liaises with internal and external clients in the tracking and status update of project plans and overall support of projects. Assists with project budgeting/forecasting. * Maintains knowledge and understanding of SOPs, client SOPs/directives, and current regulatory guidelines. * Assists in business development and pricing of projects for the department. * Evaluates client needs in relationship to overall project timelines, quality and delivery. * Engages other project team members, functional units and/or management as necessary to deliver final product, and resolve/mitigate identified issues or barriers to delivery as needed. Education and Experience Required * Bachelor's degree or equivalent and relevant formal academic / vocational qualification Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years). * In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills and Abilities * Good English language (written and oral) communication skills as well as local language where applicable Good attention to detail and quality as well as editorial/proofreading skills * Good interpersonal skills to work effectively in a team environment * Good computer skills including the use of Microsoft Word, Excel, Power Point; capable of learning new technologies * Basic organizational, time management, and planning skills to create and follow timelines, conduct long-range planning, adapt to changing priorities and handle multiple projects * Good negotiation skills * Capable of working independently with direction and exercising independent judgment * Capable of independently assessing sponsor regulatory needs and working with project team members in producing compliant deliverables * Basic knowledge of global/regional/national country requirements/regulatory affairs procedures for clinical trial authorization, licensing, lifecycle management * Basic understanding of medical terminology, statistical concepts, and guidelines * Good analytical, investigative and problem-solving skills * Capable of interpreting data PPD is an inclusive equal employment opportunity company. We value all people regardless of background, experience and abilities. PPD values the health and well-being of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role * Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner. * Able to work upright and stationary for typical working hours. * Ability to use and learn standard office equipment and technology with proficiency. * Able to perform successfully under pressure while prioritizing and handling multiple projects or activities. * May require travel. (Recruiter will provide more details.)

The company: Our client is one of the largest specialist data focused contract research companies in Europe supporting human clinical trials developing new life saving drugs. Using its innovative Electronic Data Collection system, ePRO mobile app and related biometrics services, the company is a market leader in the healthcare arena. The role will involve: * Performs Lead SAS® Programming activities to contractual requirements, project scope and to agreed timelines according to company Standard Operating Procedures. * Working closely with Members of Data Management, Project Management, Statistics, Medical Writer and Quality Assurance functions. * Acting as Lead Programmer across multiple studies * Creation of CDISC compliant SDTM and ADaM programs and supporting documentation * Senior role will include project leadership activities * Development, maintenance and validation of SAS® programs for the production of analysis datasets and tables, figures and listings for inclusion in clinical study reports * Creation and review of shells for tables, figures and listings from a programming perspective * Development, maintenance and validation of SAS based utilities * Data capture design review and input into data standards * Contributing to SQN's development of new systems, processes and SOPs The ideal candidate will have: * Expertise in CDSIC standards, including a thorough understanding of SDTM/ ADaM IG, creation of SDTM and ADaM mapping specifications, defines and reviewer's guides. * Experience in the conversion of data sets into SDTMs * Experience of running data integration projects * Strong analytical, programming and data interpretation skills * Minimum of 5-6 years SAS® programming experience ideally in the CRO environment * Good organisational skills with the ability to proactively prioritise projects and allocated activities * Experience of leading project teams, forecasting work and assessing progress * Budgeting and resourcing skills * Leadership and mentoring skills * Commercial awareness * Practical experience with SAS v 9 and macro development * Understanding of clinical development processes * Good communication skills and high level of English language

PLEASE SUBMIT ENGLISH LANGUAGE RESUMES ONLY *Various Seniority Levels * Home-Based/Remote Based Contract Opportunity *Full Time (FTE 1.0) *6+ month duration Do you prefer flexible work options that allow you to work as a contractor, while also being immersed in the PPD Culture? Apply today to learn more about current and upcoming contractor opportunities through our Functional Service Partnership team. Functional Service Partnership Homepage: Position Summary Provides technical/project leadership over a region(s), providing innovative solutions including regulatory affairs expertise and client interface to provide strategic regulatory intelligence, and guidance supporting product development from preclinical through registration and product optimization. Provides strategic, expedient and efficient preparation of client deliverables that meet current local, regional and ICH regulatory and technical requirements. Acts as liaison with internal and external clients in the provision and marketing of these services. *Qualifications:* Essential Functions * Provides senior review and advice to prepare regional regulatory submissions and ensure high quality standards that meet or exceed client expectations, local and regional requirements. * Acts as subject matter expert in providing regulatory strategy advice and technical expertise to internal and external clients and for key client projects of moderate to high complexity. Provides internal clients with up-to-date legislation and guidance as it becomes available. * Ensures quality performance for key/managed projects. * Manages project budgeting/forecasting functions. * Identifies and recognizes out of scope activities in a contract in a timely manner and liaises with other departments to follow through on all aspects of contract modifications. * Collaborates with business development in pricing and securing new business by making presentations to clients, and develops proposal texts and budgets in collaboration with other departments. * Provides matrix/project leadership, training and guidance to junior team members. * Ensures compliance with relevant organizational and regulatory SOPs and WPDs. * Participates in launch meetings, review meetings and project team meetings. Education and Experience * Bachelor's degree or equivalent and relevant formal academic / vocational qualification Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 9+ years). * In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills, and Abilities * Excellent English language (written and oral) communication skills as well as local language where applicable * Excellent attention to detail and quality as well as excellent editorial/proofreading skills * Exceptional interpersonal skills to work effectively in a team environment and act as a liaison with other departments * Advanced computer skills including the use of Microsoft Word, Excel, Power Point; capable of learning new technologies * Strong organizational, time management, and planning skills to create and follow timelines, conduct long-range planning, adapt to changing priorities and handle multiple projects * Excellent negotiation skills * Capable of working independently and exercising independent judgment to assess sponsor regulatory needs and work with project team members to producing compliant deliverables * Excellent understanding of global/regional/national country requirements/regulatory affairs procedures for clinical trial authorization, licensing, lifecycle management; expert knowledge of ICH and other global regulatory guidelines; advanced understanding of a regulatory specialty areas, such as preclinical, clinical, CMC, publishing, etc. * Superb understanding of medical terminology, statistical concepts, and guidelines * Excellent analytical, investigative and problem-solving skills * Excellent understanding of budgeting and forecasting PPD is an inclusive equal employment opportunity company. We value all people regardless of background, experience and abilities. PPD values the health and well-being of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role * Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner. * Able to work upright and stationary for typical working hours. * Ability to use and learn standard office equipment and technology with proficiency. * Able to perform successfully under pressure while prioritizing and handling multiple projects or activities. May require travel. (Recruiter will provide more details.)

We are an innovative FinTech business, and one of the biggest players in the non-standard finance sector, who are expanding our Marketing team by appointing a fully remote UX focused Digital marketing Executive to impact the customer journey across multiple brands. Our newly created group Marketing team have a brand-new opportunity for a UX Marketing Executive to join them at an exciting time of transformational change. Learning from a team of experts in the field, you will be our dedicated UX expert and will play a key role in supporting business growth through monitoring, reporting and optimising conversion. What's more you'll have a real opportunity to make this role your own and work cross-functionally across multiple existing and new brands to engage and inspire different audiences. Benefits Opportunity to join a growing financial business undergoing significant digital diversification Fully remote role, UK based Great incentives including life assurance, long service awards, health cash plan, company share scheme, pension up to 7 % matching contribution, 25 days holiday, option to buy and sell holidays, cycle to work scheme, Perkbox membership providing 200 perks, discounts and freebies…. Key responsibilities As our UX Marketing Executive, you will have a direct impact on optimising the customer journey and impacting the customer volume. Key responsibilities will include: Drive customer acquisition and retention through improving customer experience. Continuously analyse the customer journey using data insights to improve the user experience. Understand and feedback on the challenges faced by customers in taking out credit products. Support the Head of Performance Marketing and the wider marketing team with customer acquisition initiatives. Build relationships with other teams with a clear focus on improving customer volume. Understanding of financial regulations impacting the industry, ensuring that these are built into the customer journey. .

We are currently seeking a Senior Data Manager with CRO, SAS, study leadership and team leadership experience to join our Client based in the East Anglia area. This is a full time, permanent position with the potential for remote working. *The Company * Our client is one of the largest specialist data focused contract research companies in Europe supporting human clinical trials developing new life saving drugs. Using its innovative Electronic Data Collection system, ePRO mobile app and related biometrics services, the company is a market leader in the healthcare arena. *The role will involve:* * Lead the development and finalisation of high-quality data management documentation e.g., Data Management Plan, Data Validation Plan, Data Transfer Specifications, CRF Completion Guidelines * Define, communicate and lead the execution of the data management project plan. * As Lead Data Manager, perform, lead and coordinate all data review and query management activities per study documentation and the project plan to produce high quality clinical data deliverables. * Through oversight and effective delegation, ensure data management activities on assigned studies are completed according within the scope of the study contract and manage progress against the study contract and project plan; Maintain accurate resource forecasts. * Perform SAE reconciliation and associated updates within agreed timelines, check for and follow up potentially unreported Serious Adverse Events (SAEs) on the clinical database. * Maintain accurate, up to date data management documentation. * Define and maintain data tracking and status information to enable accurate assessment and reporting of study status internally and with the sponsor. * Maintain and takes responsibility for the execution of data management activities per the project plan. * Prepare and participate in client and in-house audits and regulatory inspections. * Develop and maintain advanced knowledge and understanding of all relevant systems and processes. * Mentor and support the development and progression of Data Associate IIs and Data Managers * Lead and contribute to the development, maintenance and delivery of data management training as and when required. * Lead and contributes to the ongoing development and process improvement of the department and across the company; Act as a Subject Matter Expert if required. *The ideal Candidate will have: * * Financial reporting * eCRF knowledge * Strong SAS knowledge * Contract research organisation industry experience * 3-4 years Data management experience * Team leadership or Mentorship experience * Study leadership experience

An exciting opportunity has become available for a Principal Medical Writer to join an innovative Global healthcare communications company at their site in the UK. *As a Principal Medical Writer you will:* * Play an active role in building strategy with clients based on their excellent knowledge * Improve core processes and manage multiple projects at any one time * Work autonomously to develop content against an agreed brief * Write content that meets physicians needs, anticipates these needs and supports the client's decision making * Work closely with account management team build client partnerships * Champions excellent standards in everything they are involved in and around them *Basic Qualifications and Experience:* * A degree in scientific, medical or life sciences field * Considerable experience working within medical writing * Prior experience within a medical communications agency * Experience writing for a variety of audiences * Experience building strong client partnerships through their work * The ability to be considered a scientific expert and give excellent strategic counsel *In Return You Will Receive:* * Competitive remuneration package * A truly inspiring working environment in a highly prestigious, global company If you have the correct skill-set or you know of any professionals who may be suitable, please do get in touch with Katie by email *Katie.jones*@[hayburysearch.com]() or phone (0). Katie is a Senior Search Consultant at Haybury Search covering Europe, UK, North America and Asia.

1. JOB SUMMARY/PURPOSE: Provides statistical leadership, direction and consulting for the design, analysis, and reporting of clinical trials. Actively leads in the design, analysis and reporting of clinical studies. Ensures Biometrics work is done with quality and is within timelines and budget. 2. MAJOR RESPONSIBILITIES: * Develops, guides in preparations of analysis plans, reporting specifications, and performs statistical analysis and interprets results * Writes and reviews statistical sections for clinical study protocols * Coordinates production of statistical and clinical reports including summary statistics, tables, listings and/or figures * Reviews work of other biostatisticians * Develops, modifies, and/or implements statistical techniques and processes for the analysis of clinical study data * Develops innovative statistical strategies in complex new areas * Provides significant input into the design, preparation and review of clinical study protocols and consults in the development of case report forms (CRFs) * Prepares randomization schedules * Provides leadership in statistical issues to the project team * Interacts with project teams and clients including preparation of bid proposals, statistical consulting, and visits to clients to discuss statistical issues * Manages department all levels of biostatistics and programming staff * QC the team's work; may occasionally need to lead studies * Works with functional and project managers to determine resources projections and project schedules * Leads BM hiring process and creates study assignments for BM staff * Provide support to Biostatistics and Programming department consulting efforts including design and protocol development for potential sponsors. 3. QUALIFICATIONS: * MS or PhD (preferred) in Statistics or Biostatistics * Progressive experience working with SAS or a comparable statistical package * Experience as a manager or team lead with statisticians and/or SAS programmers * Experience with the statistical aspects of a Phase I-III clinical trial * Proficient oral communication and presentation skills 4. LEADERSHIP COMPETENCIES: * Demonstrates ethics and integrity * Displays drive and purpose * Exhibits leadership stature * Holds self and others accountable for measurable high-quality, timely, and cost-effective results * Adapts to an ever-changing environment * Develops new insights into situations and questions conventional approaches * Develops networks and builds alliances; collaborates across boundaries to build strategic relationships and achieve common goals * Perceives organizational and political reality and acts accordingly * Formulates objectives and priorities, and implements plans consistent with the long-term interest of the organization * Takes a long-term view and builds a shared vision with others

With a strong background and extensive Merchandise Planning experience, you will be equipped and ready to lead the merchandise function. Having operated at a similar level in a related business (preferably multi-channel and multi-market), you'll play a key role in growing our clients business further. You'll be highly analytical, have fantastic leadership and management skills and be an excellent ...... click apply for full job details

At Ramsay Health Care we put our patients at the heart of everything we do. We firmly believe in the ethos of "People caring for People" and want to enable our teams and our patients to have the very best experience when they receive care through Ramsay services.The role:We are looking to recruit an experienced Data Protection Officer (DPO) to monitor compliance and data practices internally and ensure the business and its functions are compliant with the GDPR and other relevant national legislation. Alongside this, the DPO will also be responsible for advising on, and where required carrying out, staff training, data protection impact assessments and internal audits. This role will be home based however a weekly presence in the London office will be expected.​​​​​​​​​​​​​​What you will be doing:Implementing measures and a privacy governance framework to manage data use in compliance with the GDPR and relevant national legislationWorking with key internal stakeholders in the review of operations and projects and related data processing to ensure compliance with data privacy lawsServing as the primary point of contact for data protection queries in the businessReviewing vendor contracts and other third party data processing and data sharing arrangements in partnership with the organisation's Procurement and Information Security functionsManaging and conducting ongoing reviews of Ramsay's privacy governance framework and regular and ad hoc reporting on data privacy compliance within the organisationSetting standards and reviewing policies and procedures globally that meet the requirements under the GDPRDeveloping and delivering privacy training to various business functions and collaborating with the Information Security function to raise employee awareness of data privacy and security issues.Coordinating, conducting and monitoring data privacy audits.Responding to and advising on data subject rights requestsWorking with designated privacy lawyers, subject matter experts or champions across the business and, where necessary, outside legal advisers to help advise on local data privacy law issues.What you will bring:Law degree or post-graduate legal qualificationAt least one data protection and/or privacy certification, such as CIPP, CIPT, CIPM, ISEB, etc. Significant PQE data privacy experienceUK data privacy law experienceSignificant experience within a compliance, legal, audit and/or risk functionDemonstrable experience in developing policy and compliance training.Experience working in a regulated industryBenefits:Contributory pension schemeAccess to the Ramsay Academy - genuine opportunities to grow, develop and specialise in your career25 days' annual leave plus the opportunity to buy/sell morePrivate Healthcare and Life AssuranceAccess to our employee Discount ProgrammeWellbeing centre and access to 24/7 employee assistance line for free advice

*Principal Biostatistician (FSP) - Home based, Europe - ₠9,000 Joining Bonus* We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD - thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients. Our Biostatistics department are passionate about being data and technically agile, and driving enhanced value for our clients and patients. Determined to improve patient health, we help PPD provide industry-leading statistical, programming and clinical pharmacology contributions through global delivery, consistent quality adherence and scientific insight. As a Prin Biostatistician (FSP) you will work directly with the client as part of their team. Executing diverse statistical tasks supporting the clinical development programs within the client setting. The tasks mainly focus on managing the statistical activities performed by the biostatistics CRO and on guaranteeing by means of thorough review outstanding statistical quality. Will be involved throughout the full clinical trial process, from study design and protocol writing, over defining the statistical analyses (SAP) to reviewing all study outputs and the CSR. *Qualifications:* *Education and Experience:* * Master degree in statistics, biostatistics, mathematics or related field with 7+ years experience * Extensive experience of statistics in a clinical trial environment. * Extensive project lead/PM experience, clearly demonstrated in previous positions * Evidence of providing expert statistical input in previous positions *Knowledge, Skills and Abilities:* * Mastery of the statistical principles underlying clinical trials * Outstanding statistical skills * Mastery of the regulatory issues associated with the reporting of clinical data in the submission process * Excellent consultative skills * Mastery of SAS® programming skills and familiarity of other statistical packages (eg StatXact, Nquery) and understanding of database structures * Superb organizational, time management, and planning skills to create and follow timelines * Capable of adapting and adjusting to changing priorities * Excellent written and verbal communication skills, including proficiency in the English language * Capable of working in a multi-disciplinary team setting * Demonstrated initiative, motivation and problem solving skills * Positive attitude and the ability to organise a team and work well with others At PPD we hire the best, develop ourselves and each other, and recognise the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD you will benefit from an award-winning learning and development programme, ensuring you reach your potential. As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD truly value a work-life balance. We've grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organisation but with a local feel. - We have a strong will to win - We earn our customer's trust - We are gamechangers - We do the right thing -We are one PPD - If you resonate with our five principles above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world's most urgent health needs, then please submit your application - we'd love to hear from you. #LI-AD1

Do you want to make a difference? This exciting opportunity cannot just change your life but someone else's! - The Company Christies Care ltd lives by its values of "do as you would be done by" which applies to all of its customers, staff and suppliers. We have been providing high quality live in care to clients across the UK for over 30 years. Rated as outstanding by the Care Quality Commission for the service it provides. - The position We are looking for a Live in carer who is willing to travel nationwide and live with their client for 2 or more weeks at a time. You will be there to help your client live their life how they want to, by assisting with; personal care, moving and handling, medication or their social activities. The role itself is like no other, improving someone's quality of life is a truly remarkable experience. You will be committed, respectful, reliable, honest and trustworthy. Our carers need to be willing to travel across the UK, work for a minimum of two weeks at time. No experience is necessary due to our award winning induction course, which all of our new carers attend. A typical day would be: · Helping your client get washed and dressed in the morning · Doing some housework · Taking them on an outing · Making their favourite dinner and enjoying it together What we offer · Family run organisation for over 30 years; our staff are welcoming, friendly and enjoy their jobs which is very important to us. · A FREE award winning, industry leading induction course (with FREE Bed and Breakfast) · 24/7 support · Guaranteed earnings · Competitive wages · Flexible working patterns to suit you Apply now for a life changing opportunity!

*Senior Manager, Biostatistics (FS) - Europe (£/₠10,000 Joining Bonus)* We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD - thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients. Our Biostatistics department are passionate about being data and technically agile, and driving enhanced value for our clients and patients. Determined to improve patient health, we help PPD provide industry-leading statistical, programming and clinical pharmacology contributions through global delivery, consistent quality adherence and scientific insight. We are currently recruiting for an experienced Manager to join our Biostatistics department in EMEA, working fully remotely in the UK or mainland Europe. As a Sr Mgr, Biostatistics you will manage a team of Statisticians and Programmers within the FSP department, as well as managing project work, either leading a large program or overseeing individual studies. Responsibilities include: * Managing staff, which includes interviewing and selection, professional development, goal setting, performance management, behavioral and technical coaching and mentoring. * Ensure effective resource and utilization management of staff. * Support and coach staff to prepare and review statistical reports, clinical study reports, integrated summaries of safety, integrated summaries of efficacy and other documents as required. * Contribute statistical methods section for integrated clinical statistical reports. * Review integrated clinical statistical reports. * Coach staff to effectively communicate with sponsors concerning project work scope and budgetary changes after reviewing with management. * Aid departmental management in process-improvement strategies. Suggest, assess, and provide leadership in the department for such initiatives. * Assure department adherence to good scientific, ethical, and regulatory standards. * May act as senior statistical reviewer when required *Qualifications:* To be considered for the role you should have the following qualifications, skills and experience: * Master's degree in statistics, biostatistics, mathematics or related field * Extensive experience of statistics in a clinical trial environment (min 8 years) * Previous line management experience - min 3 years * Ability to mentor, coach and develop staff * Previous experience interviewing internal and external candidates * Excellent understanding of the statistical principles underlying clinical trials * Excellent statistical skills * Excellent understanding of the regulatory issues associated with the reporting of clinical data in the submission process * Great consultative skills * Outstanding SAS® programming skills and familiarity of other statistical packages * Excellent organizational, time management, and planning skill * Excellent written and verbal communication skills, including proficiency in the English language At PPD we hire the best, develop ourselves and each other, and recognise the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD you will benefit from an award-winning learning and development programme, ensuring you reach your potential. As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD truly value a work-life balance. We've grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organisation but with a local feel. - We have a strong will to win - We earn our customer's trust - We are gamechangers - We do the right thing -We are one PPD - If you resonate with our five principles above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world's most urgent health needs, then please submit your application - we'd love to hear from you. #LI-AD1

PLEASE SUBMIT ENGLISH LANGUAGE RESUMES ONLY *Various Seniority Levels * Home-Based/Remote Based Contract Opportunity *Full Time (FTE 1.0) *6+ month duration Do you prefer flexible work options that allow you to work as a contractor, while also being immersed in the PPD Culture? Apply today to learn more about current and upcoming contractor opportunities through our Functional Service Partnership team. Functional Service Partnership Homepage: Position Summary Provides operational leadership for the department, overseeing innovative solutions including regulatory expertise and client interface to provide strategic regulatory intelligence and guidance for product development from preclinical through registration and product optimization. Manages projects and participates in strategic initiatives. Acts as liaison with internal and external clients in the provision and marketing of regulatory services. *Qualifications:* Essential Functions * Manages staff, which may include interviewing and selection, job description preparation, professional development, goal setting, performance management, behavioral and technical coaching and mentoring, employee counseling, and separations. Approves courses of action on salary administration, hiring, corrective action, and terminations. Reviews and approves time records, expense reports, requests for leave, and overtime. Promotes all aspects of PPD Equal Employment Opportunity policy and Affirmative Action Plan. Assures department adherence to good ethical and regulatory standards. * Provides regulatory consulting and strategic advice to internal and external clients to determine the most appropriate regulatory and product development strategy for their products. Provides project specific strategy, technical expertise and coordination oversight for key client's projects. Serves as the executive contact for key clients for all issues, including attendance at regulatory authority meetings and other public relation functions. Ensures quality performance for key/managed projects. * Oversees project budgeting/forecasting to include creative input as to shifting of resources, allocations etc. to respond to a change in scope of personnel requirements to stay within project budget. Leads and participates in project meetings. * Ensures identification of out of scope activities in a contract in a timely manner and liaises with other departments to follow through on all aspects of contract modification. * Collaborates with business development and senior management in pricing and securing new business by making presentations to clients, developing and reviewing bid proposal texts and budgets and conducting contract negotiation through to closure with the client and BD. Actively engages in business development activities looking to attract collaborative and stand-alone projects. Pursues existing clients who have a need for services to win more business. * Contributes to development and implementation of global/regional function/plans. * Ensures compliance with relevant organizational and department SOPs and WPDs * Develops strategy and leads the development and implementation of processes and procedures to increase productivity and accuracy within the team. * Participates in developing and implementing systems and tools to continually improve efficiency of all activities supporting and facilitating process improvements, reduction in cycle times, submission activities, metrics and other key performance indicators. Education and Experience Required * Bachelor's degree or equivalent and relevant formal academic / vocational qualification Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 12+ years). 5+ years of management responsibility Strong leadership skills * In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills, and Abilities * Superior English language communication and negotiation skills, as well as local language where applicable, both oral and written * Excellent understanding of global/regional/national country requirements and regulatory affairs procedures for clinical trial authorization, licensing and lifecycle management; superior understanding of ICH and other global regulatory guidelines; advanced knowledge of at least one of the regulatory specialty areas: preclinical, clinical, CMC, publishing, etc. * Advanced understanding of budgeting and forecasting with the ability to interpret data with attention to detail and analytical and investigative skills * Capable of supervising, evaluating, and mentoring departmental personnel, as well as delegating tasks and facilitating the completion of assignments * Capable of driving innovation in developing new ideas related to process improvements * Excellent organizational, judgment, analytical, decision-making and interpersonal skills to manage complex projects in parallel and manage rapidly changing priorities * Effective computer skills, including the use of Microsoft (MS) Word, MS Excel, Adobe Acrobat, etc. * Capable of independently assessing sponsor needs and working with project team members in producing compliant deliverables * Capable of independently learning new technologies * Capable of effectively acting as a liaison with other departments PPD is an inclusive equal employment opportunity company. We value all people regardless of background, experience and abilities. PPD values the health and well-being of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role * Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner. * Able to work upright and stationary for typical working hours. * Ability to use and learn standard office equipment and technology with proficiency. * Able to perform successfully under pressure while prioritizing and handling multiple projects or activities. * May require travel. (Recruiter will provide more details.)

Description Kick-start your live-in carer career with Miracle Workers Agency! We are very busy in these uncertain times especially amongst the elderly and vulnerable community. We provide support for our clients in their own homes all around the UK. Attend our FREE 5 day residential course. You must be available to work for a minimum of 4 weeks. We place live-in carers with our clients throughout the UK, for variable lengths of time, thus offering you flexible work to fit in with any travel plans. Duties will include: personal care, food preparation, light household duties, shopping, recording of financial transactions, companionship and support. MWA Live-in Carer benefits include: Very competitive salary (from £630 to £700 per week at a minimum, plus double pay for bank holidays). Free 5 day residential training (you pay for your accommodation, meals, DBS and books). Flexible working assignments, thereby allowing breaks to travel, relax, get back to your own life. Free accommodation, food and travel (to clients) during your placements, therefore reducing your bills. On-going support via phone and social media from our Care Managers. All applicants must be over 25 (for insurance purposes), be eligible to work in the UK, have a full driving licence and good cooking skills. Care experience is not necessary.

PLEASE SUBMIT ENGLISH LANGUAGE RESUMES ONLY *Various Seniority Levels * Home-Based/Remote Based Contract Opportunity *Full Time (FTE 1.0) *6+ month duration Do you prefer flexible work options that allow you to work as a contractor, while also being immersed in the PPD Culture? Apply today to learn more about current and upcoming contractor opportunities through our Functional Service Partnership team. Functional Service Partnership Homepage: Position Summary Provides innovative solutions including regulatory expertise and client interface to provide strategic intelligence, and guidance supporting product development from preclinical through registration and product optimization. Provides strategic, expedient and efficient preparation of client deliverables that meet current local, regional and ICH regulatory and technical requirements. Acts as liaison with internal and external clients in the provision and marketing of these services. *Qualifications:* Essential Functions * Supports the preparation of documentation and submissions under guidance. * Coordinates and manages client deliverables supporting regulatory compliance. * Liaises with internal and external clients in the tracking and status update of project plans and overall support of projects. Assists with project budgeting/forecasting. * Maintains knowledge and understanding of SOPs, client SOPs/directives, and current regulatory guidelines. * Assists in business development and pricing of projects for the department. * Evaluates client needs in relationship to overall project timelines, quality and delivery. * Engages other project team members, functional units and/or management as necessary to deliver final product, and resolve/mitigate identified issues or barriers to delivery as needed. Education and Experience Required * Bachelor's degree or equivalent and relevant formal academic / vocational qualification Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years). * In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills and Abilities * Good English language (written and oral) communication skills as well as local language where applicable Good attention to detail and quality as well as editorial/proofreading skills * Good interpersonal skills to work effectively in a team environment * Good computer skills including the use of Microsoft Word, Excel, Power Point; capable of learning new technologies * Basic organizational, time management, and planning skills to create and follow timelines, conduct long-range planning, adapt to changing priorities and handle multiple projects * Good negotiation skills * Capable of working independently with direction and exercising independent judgment * Capable of independently assessing sponsor regulatory needs and working with project team members in producing compliant deliverables * Basic knowledge of global/regional/national country requirements/regulatory affairs procedures for clinical trial authorization, licensing, lifecycle management * Basic understanding of medical terminology, statistical concepts, and guidelines * Good analytical, investigative and problem-solving skills * Capable of interpreting data PPD is an inclusive equal employment opportunity company. We value all people regardless of background, experience and abilities. PPD values the health and well-being of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role * Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner. * Able to work upright and stationary for typical working hours. * Ability to use and learn standard office equipment and technology with proficiency. * Able to perform successfully under pressure while prioritizing and handling multiple projects or activities. * May require travel. (Recruiter will provide more details.)

This is a great opportunity for a Senior Statistician to join one of the largest specialist data focused contract research companies in Europe supporting human clinical trials developing new life saving drugs. The specialist clinical biometrics CRO is supporting global pharma, biotech, medical device and animal health partners with innovative clinical development services. *The Company * Our client is one of the largest specialist data focused contract research companies in Europe supporting human clinical trials developing new life saving drugs. Using its innovative Electronic Data Collection system, ePRO mobile app and related biometrics services, the company is a market leader in the healthcare arena. *The role will involve:* * Responsible for managing the statistical aspects of assigned projects completed * Accountable for the timely, reliable and appropriate processing of the statistical evaluations, in compliance with the United Kingdom Statutory Instrument 2004 No 1031 The Medicines for Human Use (Clinical trials) Regulation 2004 and its subsequent amendments, ICH Guidelines for Good Clinical Practise and other national and international standards and legislation as required, Standard Operating Procedures (SOPs) and client instructions. * You will work closely with Study team members (statisticians, SAS programmers, CRF designers, data managers, project managers, medical writers), as well as Information Technology (IT), Quality Assurance (QA) functions, and the business development group. * Input into Quotations, * Provision of Statistical Expertise for Clients. * Overseeing and Contributing To SAS® Programming. * Performing the Role of Study Project Manager on Designated Studies. * Contribute to Process Improvement Initiatives, And the Review of Process Documents. *The ideal Candidate will have: * * Contract Research Organisation experience * Previous Senior Statistician experience * Project work * Project Management and Client Coordination * Training * Business Development * Process Development * Statistical Consultancy

Board Members, National Housing FederationLocation: NationwideMake your expertise countThe National Housing Federation (NHF) is the voice of housing associations in England. We are the trade body to almost 600 housing associations - not for profit social landlords who provide 2.6 million homes to around 6 million people. We are proud to be at the forefront of tackling the nation's housing crisis.Our vision is for a country where everyone can live in a good quality home they can afford, and we are looking for a board member who is committed to helping us achieve this. Three of our board members are coming to the end of their terms and we are looking to appoint to the vacant posts. Our board members come from both within and outside of the social housing sector. With three posts to fill, we have an opportunity to bring more diverse experience to the board and therefore we invite applications from people with a range of expertise. The areas of expertise we are seeking to attract to the board includes:- Housing-Health or social care- Homelessness- Service provision in areas of deprivation (levelling up)-Political links relevant to current housing policy-Equality, diversity and inclusion - Investment/corporate finance-Energy/zero carbon agenda- Digital expertiseYou will have a record of achievement in one of the areas above. Your experience may come from within or outside the social housing sector.As a successful board member, you will provide excellence in governance, be an ambassador and use your strategic skills to make us an even more effective organisation. You will be involved in influencing the NHF's business to ensure that we successfully manage the challenges and significant change that the future is set to bring. In addition to the above, essential experience required includes:-A proven strategic leadership, vision and a collegiate approach.-Governance expertise and strong analytical skills.-A track record of effective stakeholder relationship management and ambassadorial activities.-A commitment to championing equality, diversity and inclusion in the social housing sector.- A passion for, and good understanding of, the social housing sectorOur current Board is not sufficiently reflective of the diversity of our members and the communities our sector exists to serve. We are especially keen to take a step towards changing this and strongly encourage applications from qualified people, regardless of protected characteristics or social background. We are a disability confident employer therefore, if you are a disabled person who demonstrates the skills and experience we consider essential for the role, we will offer you an interview.Board meetings are generally held in central London (currently held by video conference) but there may be occasional national travel. Time commitment from board members is approximately seven to ten days a year. If you believe in our work and understand the value of exceptional governance, we would love to hear from you.Please note that due to social distancing measures, interviews are likely to take place by video conference, although this will be kept under review. Closing date: 25 April 2021Interview date: 9 or 10 June 2021

I am working with a leading security systems organisation who are looking for a Digital Learning Manager to join them on a permanent basis to help manage their existing team and drive their learning strategy to the next level. My client is globally renowned for their monopolisation of this industry, not only in revolutionising the use of technology but also in terms of how they implement digital le...... click apply for full job details

ERP Trainer My local government client is looking for a trainer with extensive experience in developing and delivering training materials as part of an ERP implementation or an ERP replacement solution, ideally within a unitary local authority setting. Key skills Experience of highly successful training delivery on HR, Payroll, Expenses, Employee/Manager Self Service or Finance, Procure to Pay, Sales...... click apply for full job details

This highly-regarded and established firm based in Brierley Hill in Dudley is looking to appoint a full-time or part-time Commercial Property Solicitor or Commercial Property Legal Executive to their market-leading commercial property department. As a Commercial Property Lawyer you will have from 2+ Years' PQE and be able to demonstrate detailed knowledge and technical expertise in dealing with complex commercial property caseloads. You will have good solid academics and be able to work effectively as a commercial property lawyer as part of the commercial property team. The firm is offering a very competitive salary and package as well as ongoing career progression opportunities. The PQE above is a guideline only and does not preclude applications from those with more or less PQE. For an informal discussion regarding this job and many more legal vacancies please contact Nadim Baig at Bewley Recruitment or send your CV to Nadim at Bewley Recruitment. Key Words: Commercial Property, Brierley Hill, Dudley, Solicitor, Legal Executive, Lawyer, Full-Time, Part-Time.

The business: International diagnostics and advisory business. The project: The business is taking responsibility for a very large number of GP Practices. There is an urgent requirement to upgrade TQuest Order Comms at two sites. All GPs from... ..... click apply for full job details

Job Title: Lead Python Developer | Machine Learning | Market Rate Location: Remote/London Salary/Rate: Market Rate Start Date: May 2020 Job Type: Contract We have an exciting opportunity now available with one of our sector-leading consultancy clients! They are currently looking for skilled Lead Phython Developers to join their team on a contract that is set to finish a the end of 2022...... click apply for full job details

Specifications Technologist Food Manufacturing London £33,000 When it comes to being a spec tech, you're a pro. You've got the retailer experience too. So why would you move into another specs role? Well, here you will get pushed on to full account management over time...... click apply for full job details

I am working with a specialist consultancy who create industry leading learning content specifically for the hospitality industry. They are looking to bring on board a brand-new position within their business which is a Compliance Consultant. There aren't many consultancies that are specialists within hospitality digital learning, but my client has completely taken control of that niche...... click apply for full job details

Frontend Engineer Description Interested in joining an organisation that is being recognised for the evolution of its products and the impact this has on clinical trial recruitment? We dare to change the status quo when it comes to helping match patients to clinical trials. We aim to accelerate the breakthroughs of new treatments by bridging the gap between medical research and the people who need th...... click apply for full job details

We are recruiting for a Senior Consultant (Cisco Switching and Routing / Wireless). The role of the Senior Consultant is to provide expert design and deployment of technical solutions and services to CAE's customers. Senior Consultants are responsible for leading technical teams to deliver complex projects from design to transition into BAU teams...... click apply for full job details

Outpatient Nurse Surrey At TTM Healthcare we are proud to have partnered with one of the leading private hospitals based in Surrey that offer a wide range of services across medical and surgical interventions. This facility is set in beautiful tranquil surroundings making it the perfect retreat for patients to recuperate. They have an available opportunity for a Staff Nurse to work in the outpatient department of the hospital with excellent experience, skills and knowledge. If you think the position is right for you, let's talk. RESPONSIBILITIES: The overall responsibility within this role to work across their busy Outpatient department, working alongside the consultants ensuring the smooth and effective running of the clinics throughout the day. CLINICAL RESPONSIBILITIES: Working alongside the Senior Staff Nurses in the unit you will be responsible for ensuring the right standard of care is provided to all patients at all time. You will have an innate ability to quickly identify any issues or concerns and act accordingly. Working as part of the team you will be competent across Venepuncture, Cannulation and Phlebotomy, carrying out these tasks on a daily basis while maintaining a safe environment for patients under your care. Part of your role with involve administrative duties such as updating clinic sheets, answering queries from patients, consultants and secretaries and booking consultant rooms. You will also work to assist the consultant during clinics including in minor procedures. You may also be required to deputise for any senior members of staff in their absence. EDUCATIONAL RESPONSIBILITIES: Nursing Degree NMC Registration REQUIREMENTS: To be eligible for the role, you will need to: • Be an NMC registered nurse with experience of working in a surgical or outpatient setting • Have a passion for high quality patient safety and care • Experience of customer care, including interacting with challenging customers and situations • Have the willingness to undergo further training and development to broaden your skill set • Be a caring and compassionate nurse with strong attention to detail and the ability to work well under pressure. • Adapt easily to new situations and be able to build strong working relationships within the team REWARDS: You will enjoy the following benefits: • Competitive Annual Salary • 33 days annual leave • Private Healthcare • Pension Scheme • Life Assurance • Child Care Vouchers • Continued Training and Development Opportunities • Subsidised Staff Restaurant • Free Off Site Parking DETAILS: Location:Surrey Job-Type:Permanent Salary:£28,000-£32,000 CONTACT: Apply now for a call back to discuss the role in more detail Ref IND CB TTM Healthcare is an Equal Opportunities Employer.

Anaesthetic Nurse Surrey At TTM Healthcare we are proud to have partnered with one of the leading private hospitals based in Surrey that offer a wide range of services across medical and surgical interventions. This facility is set in beautiful tranquil surroundings making it the perfect retreat for patients to recuperate. They have an available opportunity for a Anaesthetic Practitioner to work in the theatre department of the hospital with excellent experience, skills and knowledge. If you think the position is right for you, let's talk. RESPONSIBILITIES: The overall responsibility within this role is to assist the anaesthetist in the administration of anaesthetic during surgery, and tasks include the preparation of equipment, monitoring the patient's condition, and reaction to instructions from the anaesthetist. CLINICAL RESPONSIBILITIES: Reporting into the Theatre manager as an Anaesthetic Nurse you will be responsible for planning and delivering appropriate care to patients on the ward. Part of your day to day as an Anaesthetic Nurse will involve preparing the Anaesthetic room according to the individual needs of the patient and Anaesthetist, ensuring all equipment is checked prior to use and any faults reported to the Theatre Co-ordinator immediately and preparing patients and provide assistance for clinical/operative procedures. You will also be responsible for updating and maintaining patient records and responding to any queries or complaints. You will also be involved in the induction of new staff & any other ad hoc duties required by senior members of staff. EDUCATIONAL RESPONSIBILITIES: Nursing Degree NMC Registration REQUIREMENTS: To be eligible for the role, you will need to: • Have you will have a relevant anaesthetic nurse qualification or operating department practitioner qualification. • At least 1 years+ experience working in anaesthetic's and experience across multiple specialties. • An innate attention to detail with a strong ability to work well under pressure. The ability to adapt easily to situations and be a good communicator within a team. • To have computer competency across healthcare related systems REWARDS: You will enjoy the following benefits: • Competitive Annual Salary • 33 days annual leave • Private Healthcare • Pension Scheme • Life Assurance • Child Care Vouchers • Continued Training and Development Opportunities • Subsidised Staff Restaurant • Free Off Site Parking DETAILS: Location:Surrey Job-Type:Permanent Salary:£32,000-£39,000 CONTACT: Apply now for a call back to discuss the role in more detail Ref IND CB TTM Healthcare is an Equal Opportunities Employer.