474 jobs found in Cambridge

Background: This forward-thinking GP surgery is offering an experienced Practice Nurse the chance to join their dedicated clinicians, who provide nothing but the best service for all patients! You will be part of the nursing team and be able to focus on your specialist interest, be that diabetes, respiratory conditions, or something else! If you have experience in long-term conditions, then this co...... click apply for full job details

Nurseplus are looking for experienced Registered Nurses to provide holistic, person-centred care to our clients. We have lots of work available for Registered Nurses in a variety of care settings including local Nursing Homes, Residential Homes, Learning Disability Units, Mental Health Units and Private Hospitals in Cambridge and surrounding areas...... click apply for full job details

Background: This forward-thinking GP surgery is seeking an Advanced Nurse Practitioner to join their team who is ready to get stuck in! The practice currently operates on a total triage basis, so you would be expected to hit the ground running with this, before seeing patients face-to-face where necessary...... click apply for full job details

The Intern Group is the leading provider of global internship programs and is regularly featured in the world's top media including CNN, Forbes, Financial Times and Bloomberg amongst other publications. Our virtual internships provide you with the opportunity to gain invaluable professional experience, grow your network and make your resume shine, wherever you are. Realize your potential with a virtual engineering internship program. This is a flexible opportunity to fit your schedule. You choose: Between 10, 20, 30 or 40 hours of remote engineering internship per week The duration of your internship - from 4 to 24 weeks The start date - we offer internship start dates every month, all-year-round Whether you're a prospective or current university student, recent graduate or professional looking to upgrade your career, a virtual internship in engineering could offer the perfect next step. What's included in the program? A 10, 20, 30 or 40 hour per week professional internship in engineering. We have placed interns with some of the most prestigious organizations in the world, through to small and medium-sized businesses and entrepreneurial start-ups, including SONY Music, KPMG, Aflac, Quintessentially, Grant Thornton and more. Best-in-class career advancement training. You will build the skills to thrive. Our training focuses on developing in you the 8 key competencies essential to succeed in the 21st century world of work. Keynote career talks from global business leaders. You will learn from the best. Our program gives you 3 months access to exclusive, real-time talks from leading speakers. A small sample includes: Nick Jellicoe, the global head of marketing and PR at Rolex for 10 years. Federico Vega, one of Latin America's highest-profile entrepreneurs. Lord Stevenson, British politician and businessman. The majority of our internships are unpaid. Our goal is to find the best possible internship placements that will provide our participants with real-world responsibilities and the skills they will need for the future. If a host organization offers a stipend or another form of compensation, participants are welcome to accept it, however, it is not guaranteed. The true focus is on the immense professional growth.

Embedded Developer required at either a graduate, junior or mid-level for a leading software business who continue to grow due to successfully landing 2 new major projects. After an incredibly successful 2020, our client is looking to expand their established development team by bringing onboard a talented Embedded Developer. The current pipeline promises a whole host of challenging yet rewarding projects over the next 12 months. This offers an incredible opportunity to be directly involved in some really impressive achievements. This Embedded Developer role would suit someone in the junior - mid-level stage of their career and we are also open to hearing from exceptional Computer Science graduates who want to achieve their first commercial role. You can expect to be directly involved in Embedded Developer projects from the outset, building commercial software products for high-value existing clients, new business but also exciting internal projects. To be successful in this role, the following knowledge & experience is key: Working knowledge of C/C++ Experience with Microchip, Cypress, or other Embedded platforms Flawless organisation skills including detailed planning and documentation. Alongside a competitive base salary, benefits include, free gym membership, incredible investment into individual Learning and Development for each employee and flexi working with the chance to be either office or home based. This is a fantastic Embedded Developer role which would see you push your career to the next level, working with a team of highly skilled engineers in a supportive and varied work environment. To apply for this Embedded Developer role please send your CV to Max Farrow at IT Recruitment Solutions. Embedded Developer, Software Developer, Mid-level Developer, Junior Developer, Graduate Developer, Embedded, C, C++, Remote Working £Competitive + Benefits

Senior Bioanalytical Programme Manager £38,000 - £50,000 Cambridge Are you a Senior Bioanalytical Programme Manager looking for your next exciting career move? Is your next career move as a Senior Bioanalytical Programme Manager going to be at a company that has a truly global reach and enables their employees to develop and strengthen their careers? If you are a Senior Bioanalytical Programme Manage...... click apply for full job details

Principal Scientist £42,000 - £52,000 Cambridge Are you a Principal Scientist looking for your next exciting position as a Principal Scientist? Do you aspire to work for a company that appreciate and even reward their team members based on their performance? Are you a Principal Scientist and want the next step in your career to be within a fast-growing, dynamic, successful team? This Principal Scient...... click apply for full job details

Avantor Services provides a broad variety of on-site Laboratory Services for major pharmaceutical customers and works collaboratively with the client to provide resource to deliver core scientific activities. Our customer, AstraZeneca, requires an individual to work within their Protein Science team as a Research Scientist...... click apply for full job details

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. If you're a strategic thinker, planner and multitasker as comfortable working independently as you are on a team in delivering compliant deliverables based on solid judgment, PPD is the place to be. Our global regulatory experts contribute the regulatory strategy and knowledge to help our clients navigate the challenging regulatory environment - and help get life-changing therapies to patients faster. As a Principal Regulatory Affairs Specialist for Chemistry, Manufacture and Controls (CMC) - lead focus on Advanced Therapies, you will provide innovative regulatory solutions to our clients. The purpose of this role is to lead and support Global Regulatory CMC projects across multiple product types with a lead focus on Advanced Therapies (Cell and Gene therapies). This role serves as the lead over several projects in providing innovative solutions including CMC regulatory expertise and client interface to provide strategic regulatory intelligence, and guidance supporting product development from preclinical through registration and product optimization. You will provide strategic, expedient and efficient preparation of client deliverables that meet current local, regional and ICH regulatory and technical requirements and act as liaison with internal and external clients in the provision and marketing of these services. Essential functions of the role specifically include: • Application of strong regulatory experience in the area of ATMP - advanced therapy medicinal products (cell and gene therapy products) and biological/recombinant products. • Preparation of EU dossier applications for genetically modified organisms (GMO) • Authoring of GMO dossiers and associated regulatory documentation • Authoring of EU IMPD and US IND Module 3 for biologics, cell and gene therapies and small molecule product types • Authoring of EMA, FDA, Health Canada, National EU RA, UK MHRA, Scientific Advice and related meeting packages • Generation of responses to agency questions. • Client project interface and project management Additionally: • You will provide senior review of regulatory documents and submissions created within or outside of the company in order to ensure high quality standards that meet or exceed client expectations, local and regional requirements. • You will act as subject matter expert in providing regulatory strategy advice to internal and external clients on projects of moderate complexity. • Provide internal clients with up-to-date legislation and guidance as it becomes available. • Participate in project management activities to support the provision of regulatory services, and act as liaison with internal and external clients in the provision of marketing these services. • Provide matrix/project leadership, training and guidance to junior team members to support understanding of regulations, impact on study, assessment of risk, etc., and to achieve a specific goal and/or project deliverables. • May provide input on performance reviews to management. • Ensures adherence to project budgets, time schedules, and scope of work. • Ensures compliance with relevant organizational and regulatory SOPs and WPDs. • Contributes to business development activities, including project budgeting/forecasting. *Qualifications:* Ideally you will have: • Application of strong regulatory experience in the area of ATMP - advanced therapy medicinal products (cell and gene therapy products) and biological/recombinant products. • Preparation of EU dossier applications for genetically modified organisms (GMO) • Authoring of EU IMPD and US IND Module 3 for biologics, cell and gene therapies and small molecule product types • Authoring of Scientific Advice and related meeting packages • Generation of responses to agency questions. • Client project interface and project management 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; expert knowledge of ICH and other global regulatory guidelines • Excellent analytical, investigative and problem-solving skills • Understanding of budgeting and forecasting 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-SH1 As we are likely to receive many applications, sometimes we are unable to provide feedback to everyone.

Senior/Regulatory Affairs Manager - Client Dedicated (CMC - Small Molecules, Biologics) 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. PPD has an exciting opportunity for a Senior/Regulatory Affairs Manager to join us exclusively for one of our strategic partners. PPD works in collaboration with this pharmaceutical partner; you will be dedicated to the client projects, processes, working within their teams and systems on behalf of PPD. In this role you will be a pivotal team member with at least 5-7 years of regulatory experience, responsible for driving and leading regulatory CMC strategy. You will provide innovative solutions including global regulatory therapeutic area expertise, strategic regulatory intelligence and guidance for product development from preclinical through registration and product optimization. You will feel confident providing regulatory advice and carry out projects in the provision of regulatory affairs services whilst acting as liaison with internal and external clients in the provision of these services. *Qualifications:* The ideal candidate will have: - 5-7 years of relevant regulatory CMC experience - Small molecules and biologics expertise - Expertise in writing CMC sections of the dossier - Experience with scientific advice attendance and writing - Proven project management experience and success building relationships across a diverse stakeholder team Knowledge, Skills and Abilities: • Excellent interpersonal skills, and oral and written communication skills • Excellent organizational and planning skills • Good negotiation skills • Ability to work on own initiative • Good judgement and decision-making skills • Ability to act as liaison with other departments where necessary 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 values 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-SH1

CK Clinical are recruiting for an Associate Director, Regulatory Affairs to join Boyds Consultants. Boyds are a consultancy providing a wide range of expertise and skills central to the development of pharmaceutical and biotechnology medicinal products and medical devices. Working with early stage biotechs, medical device companies and universities, the team supports the development of advanced therapy medicinal products (ATMPs), small molecules and biologics across a wide range of therapeutic areas. This is a permanent position to join their award-winning Regulatory team. Remote working can be considered, with occasional visits to site in Cambridge or Crewe. *Responsibilities:* As Associate Director, Regulatory Affairs you will independently lead projects to develop, review and execute regulatory strategy for clients, and will also take the lead delivering regulatory activities/submissions necessary to support product development and registration. *Key duties will include:* - Providing expert strategic advice to clients, taking into account regulations and guidelines relevant to their products. - Preparation of regulatory submission documents including orphan drug designation applications, scientific advice briefing documents, CTA/INDs, paediatric investigation plans, PRIME/BTD and MAA/NDAs. - Lead regulatory agency interaction and negotiations. - Provide support to the wider business, potentially including mentoring and business development. - Be a leader in developing new procedures/processes for complex ATMPs. *Qualifications:* As Associate Director, Regulatory Affairs you will require: - At least a Life Sciences degree. - Proven Regulatory Affairs experience within the pharmaceutical industry and product development. Experience within consultancies is a bonus. - Experience working with ATMPs is essential. - Extensive experience leading the development of Regulatory Strategy. - Strong experience with EU and US submissions and regulations. - Ability to lead Health Authority interactions. - Self-starter attitude, with the ability to independently find creative solutions for complex problems. *Apply:* Entitlement to work in the UK is essential. Please quote reference 50069 in all correspondence. CLINBOYD

Are you a strategically focussed Regulatory professional and would like to play an integral part in bringing life changing Oncology medicines to patients? If you are please read on.. At AstraZeneca work with diverse minds, all united by a shared passion to learn, grow and discover. Within *Oncology Regulatory Science and Strategy (ORSS)* we bring hope and solutions to patients with unmet needs across the globe. As Regulatory professionals working on Oncology products, we work in areas of unmet need and take innovative regulatory approaches to bring life-changing treatments to patients. We work across our pipeline and the business to get medicines to patients as efficiently and effectively as possible. The *Senior Regulatory Affairs Director (SRAD)* serves as the *Franchise Global Regulatory Lead* *(GRL)* on *complex programs with multiple indications*. You will *lead the development and implementation of the global regulatory strategy for a product/group of products of increasing complexity*. In addition to GRL responsibilities, the SRAD has the ability to function in dual capacity by also serving as a regional lead based on their location. You will ensure that the strategy is designed to deliver rapid approval with competitive labelling in keeping with the properties of the product(s) and the needs identified by the business, markets and patients. You'll provide *team leadership and participate in coaching, and mentorship* to members of the large Global Regulatory Strategy Team and will be responsible for delivery globally to contribute to the global project team's deliverables. The SRAD establishes external relationships with key regulatory stakeholders, leveraging these to maintain competitive advantage. You will be viewed as a senior leader within the regulatory community. *Typical Accountabilities, what you will be doing:* * Accountable for leading the development and implementation of the global regulatory strategy for a product/group of products of increasing complexity or spanning multiple indications. This includes providing Regulatory leadership on franchise products with multiple indications and development programs. May also serve as a regional Regulatory Affairs Director (RAD) depending on location. * Ensure that the strategy is designed to deliver rapid approval with competitive labeling in keeping with the properties of the product(s) and the needs identified by the business, markets and patients. * Lead a Global Regulatory Strategy Team (GRST) of other GRLs responsible for specific indications/programs within the franchise, key contributing members from the regions, emerging markets, RA CMC, Labelling and members of the submission and execution team. Participate in coaching, and performance feedback to members of your GRST. * Lead the objective assessment of emerging data against aspirations and update senior management on project risks/mitigation activities. * Represent Regulatory Affairs on Global Product Teams (GPTs) providing strategic regulatory advice and accountable for all Regulatory activities * Accountable for the delivery of all regulatory milestones on your team including assessment of the probability of regulatory success based on a thorough assessment of regulatory risks and mitigations. You will lead preparation of the regulatory strategy document and target product labelling. * Demonstrate strategic leadership skills thereby contributing to effective product development. * Participate in and promote novel regulatory initiatives internally, and engage externally on the corresponding topics as needed. Lead the development of novel regulatory tools and technology. * Ensure appropriate planning and construction of the global dossier and core prescribing information led by the respective teams. Accountable for product maintenance, supply and compliance activities associated with marketed brands. * Partner with marketing companies (countries) and regional regulatory affairs staff to influence developing views/guidance. *Education, Qualifications, Skills and Experience:* *Essential:* * An advanced degree in a science related field and/or other appropriate knowledge/experience. * Previous demonstrated experience of regulatory drug development including product approval/launch. Successful leadership to at least one major regulatory approval at a global level including leading response team and labeling negotiations is desired. * Previous experience in leading major health authority interactions. * Solid knowledge of regulatory affairs within several therapeutic areas in early and late development. * Broad background of experience working in pharmaceutical business and prior experience in several areas within regulatory affairs. Experience in relevant therapy area (small molecules & biologics) is preferred. * Proven leadership experience. * Ability to think strategically and critically and evaluate risks to regulatory activities. * Deep understanding of global regulatory science and will integrate with project strategy. You have a long standing experience of overall drug/biologic development processes and strategies for high profile, complex or novel development programs. *Desirable:* * Previous experience with FDA advisory committee and EMA oral explanation would be a plus * Previous experience working on due diligence activities and in a business alliance environment. * Ability to work strategically within a complex, business critical and high-profile development program. *Location:* Cambridge, UK *Salary:* Competitive + Excellent Benefits *Closing Date:* 30th April 2021 Next steps, if the role looks suitable to you please apply! *Where can I find out more?* Our Social Media, Follow AstraZeneca on LinkedIn []() Follow AstraZeneca on Facebook []() Follow AstraZeneca on Instagram []()

Senior Regulatory Consultant This is a great opportunity to join a company of over 200 dedicated Regulatory Affairs experts offering consulting services to global clients across the life sciences sector including pharmaceuticals, biotechnology and medical devices. The position is a permanent role, offering a great career growth plan and exposure to multiple RA projects in various products including...... click apply for full job details

Are you a strategically focussed Regulatory professional and would like to play an integral part in bringing life changing Oncology medicines to patients? If you are please read on... At AstraZeneca work with diverse minds, all united by a shared passion to learn, grow and discover. Within *Oncology Regulatory Science and Strategy (ORSS)* we bring hope and solutions to patients with unmet needs across the globe. As Regulatory professionals working on Oncology products, we work in areas of unmet need and take innovative regulatory approaches to bring life-changing treatments to patients. We work across our pipeline and the business to get medicines to patients as efficiently and effectively as possible. *The Regulatory Affairs Director (RAD)* provides *strategic and operational regulatory leadership to the development, commercialisation and life cycle management of assigned product(s)*. You will serve as the *global regulatory lead (GRL) on early stage projects or specific indications of larger programs, or as regional regulatory lead*. You'll contribute significantly to overall product and clinical strategy. The role plays a key role *influencing regulatory authorities* through regular contacts to improve regulatory outcomes. The RAD *leads cross-functional teams in major regulatory submissions (NDA, IND/CTA)*, *health authority interactions, label discussions, and securing NDA/BLA approvals.* As a GRL, the RAD leads the Global Regulatory Strategy Team (GRST) in formulating Global Regulatory strategy and delivering on NDA Filings and Approvals. Alternatively, as a regional regulatory lead, the RAD is a member of the GRST and is accountable for providing the region-specific Regulatory strategy and advice. The RAD serves as the face of the company with health authorities. *Typical Accountabilities, what you will be doing:* * Accountable for leading the development and implementation of the regional or global regulatory strategy for a product/group of products. Ensures that the strategy is designed to deliver rapid approval with competitive labeling in keeping with the properties of the product(s) and the needs identified by the business, markets and patients. This includes health authority engagement strategy and considerations of expedited regulatory programs. * Lead cross-functional Teams in major health authority interactions. This includes setting the strategy and planning for the interaction, driving the formulation of the briefing document focused on strategy and scientific content, leading the team through meetings rehearsals, and moderating the meeting itself. * Lead a Global Regulatory Strategy Team (GRST) of key contributing members from the regions, emerging markets, RA CMC, Labelling and members of the submission and execution team. Participate in coaching, and performance feedback to members of your GRST. * May (depending on role and project) represent Regulatory Affairs on Global Product Teams (GPTs) providing strategic Regulatory advice and be accountable for all Regulatory activities * Accountable for the delivery of all regulatory milestones on your team including assessment of the probability of regulatory success based on a thorough assessment of regulatory risks and mitigations. Lead preparation of the regulatory strategy document and target product labeling. * Demonstrate strategic leadership skills contributing to effective product development. Provide team leadership and participate in coaching, and performance feedback to members of the GRST. * Accountable for initiating and delivering key regulatory documents and plans and leading the negotiations with health authorities. * Lead the objective assessment of emerging data against aspirations and update senior management on project risks/mitigation activities. * Ensures appropriate planning and construction of the global dossier and core prescribing information led by the respective teams. Accountable for product maintenance, supply and compliance activities associated with marketed brands. * Partner with marketing companies (countries) and regional regulatory affairs staff to influence developing views/guidance. *Education, Qualifications, Skills and Experience:* *Essential:* * An advanced degree in a science related field and/or other appropriate knowledge/experience. * Previous demonstrated experience of regulatory drug development or equivalent, and experience with major Health Authority interactions. Prior experience with phase 3 design including end of phase 2 health authority interactions is desired. Contribution to a regulatory approval including leading response team and labelling negotiations would be a plus. * A solid knowledge of regulatory affairs within at least one therapeutic area in early and late development. * Demonstrated competencies of strategic thinking, strategic influencing, innovation, initiative, leadership and excellent oral and written communication skills. * The ability to think strategically and critically and evaluate risks to regulatory activities. *Desirable:* * A good understanding of guiding principles in drug development such as benefit/risk profile, dose selection or statistical design. * Broad background of experience working in pharmaceutical business and prior experience in several areas within regulatory affairs. Experience in relevant therapy area (small molecules & biologics) is preferred. * Ability to work strategically within a complex, business critical and high-profile development program. * Critical thinking on current global regulatory science questions and good understanding of the corresponding scientific and clinical components *Location:* Cambridge, UK *Salary:* Competitive + Excellent Benefits *Closing Date:* 30th April 2021 Next steps, if the role looks suitable to you please apply! *Where can I find out more?* Our Social Media, Follow AstraZeneca on LinkedIn []() Follow AstraZeneca on Facebook []() Follow AstraZeneca on Instagram []()

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. If you're a strategic thinker, planner and multitasker as comfortable working independently as you are on a team in delivering compliant deliverables based on solid judgment, PPD is the place to be. Our global regulatory experts contribute the regulatory strategy and knowledge to help our clients navigate the challenging regulatory environment - and help get life-changing therapies to patients faster. We have a position open for a Regulatory Affairs Manager. This role provides technical/project leadership across regions, 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. The role also provides strategic, expedient and efficient preparation of client deliverables that meet current local, regional and ICH regulatory and technical requirements, and acts as liaison with internal and external clients in the provision and marketing of these services. Responsibilities: * Provide senior review and advice to prepare regional regulatory submissions and ensure high quality standards that meet or exceed client expectations, local and regional requirements. * Act 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. * Ensure quality performance for key/managed projects. * Manage project budgeting/forecasting functions. * Identify and recognize out of scope activities in a contract in a timely manner and liaise with other departments to follow through on all aspects of contract modifications. * Collaborate with business development in pricing and securing new business by making presentations to clients and developing proposal texts and budget in collaboration with other departments. * Provides matrix/project leadership, training and guidance to junior team members. * Ensure compliance with relevant organizational and regulatory SOPs and WPDs. * Participate in launch meetings, review meetings and project team meetings. *Qualifications:* Job Qualification What the role requires you to have: • Bachelor's degree or advanced degree preferred, or equivalent and relevant formal academic / vocational qualification • Previous experience that provides the knowledge, skills, and abilities to perform the job, at least 5 years. • Proven project management experience, and experience performing effectively in a client facing 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 speciality 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 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.

Senior Flow Cytometry Scientist Melbourn £30,000 - £42,000 Are you a Flow Cytometry Scientist or a Senior Flow Cytometry Scientist looking for your next exciting career progression opportunity within a fast-growing, dynamic, successful team? Do you aspire to work for a company that appreciate and even reward their team members based on their performance? Are you a Senior Flow Cytometry Scientist look...... click apply for full job details

North Cambridge Part-time- circa 20-28 hours per week Salary: £40-45,000 pro-rata + 15% bonus, g enerous pension scheme and many other benefits The biggest attraction of this senior role by far is the exceptional working environment and the career prospects on offer. The level of responsibility and career opportunity will grow ...... click apply for full job details

Regulatory Affairs Specialist/Senior Regulatory Affairs Specialist - Publishing/Submissions - Home Based EMEA 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. If you're a strategic thinker, planner and multitasker as comfortable working independently as you are on a team in delivering compliant deliverables based on solid judgment, PPD is the place to be. Our global regulatory experts contribute the regulatory strategy and knowledge to help our clients navigate the challenging regulatory environment - and help get life-changing therapies to patients faster. As a Regulatory Affairs Specialist/Senior Regulatory Affairs Specialist, you will electronically publish regulatory documents and submissions via electronic gateways using submission publishing tools. Seeking candidates with experience using Adobe Acrobat, Adobe Acrobat Plug Ins and other submission publishing tools. Summarized Purpose: Provides strategic, expedient and efficient preparation of client electronic submission deliverables and dossiers that meet current local, regional and ICH regulatory and technical requirements. Ensures successful regulatory review outcomes for product milestones. Serves in a technical quality review role and is responsible for the thorough review of published documents and submissions created within or outside of PPD to ensure quality of standards meet regulatory compliance requirements and meet or exceed client expectations. Essential Functions: Provides client electronic submission deliverables supporting regulatory compliance Prepares components of electronic regulatory submissions that meet the electronic document requirements set by regulatory guidance, publishing documents and submissions that work with sponsor and/or regulatory agency software programs, and meeting consistency and data security issues Maintains document lifecycle for submissions Supports development and implementation of project-specific processes for sponsors with unique technology requirements and may act as the PPD liaison for regulatory submission with the sponsor and assist PPD project teams in executing regulatory submission strategies Provides mentoring of other regulatory publishing personnel, as needed Uses professional judgment to evaluate the regulatory publishing needs in relationship to the overall project timelines, quality and delivery Engages other project team members, functional units or publishing management as necessary to deliver final product and resolve/mitigate identified issues or risk to delivery Acts independently within a project team or as the project team lead to evaluate and deliver publishing tasks *LI-SH1 *Qualifications:* Education and Experience: Bachelor's degree or equivalent and relevant formal academic / vocational qualificationPrevious experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years). Knowledge, Skills and Abilities: Working knowledge of global regulatory requirements and guidances for submission requirements, document management, document publishing and electronic submissions Advanced knowledge of Microsoft (MS) Word, MS Excel, Adobe Acrobat, electronic document management systems, document publishing tools, publishing systems, eCTD validation and viewing tools Advanced knowledge of electronic templates and skilled in formatting and troubleshooting templates Ability to manage several complex projects in parallel and adapt to changing priorities Ability to exercise independent judgment in developing methods, techniques and evaluation of criteria using defined procedures and practices Ability to independently assess sponsor needs and work with project team members in producing compliant deliverables Ability to independently learn new technologies Excellent organizational skills and effective interpersonal skills Excellent analytical ability and problem-solving capabilities Good working knowledge of medical terminology, statistical concepts, and guidelines and requirements of the FDA and other international regulatory agencies Excellent editorial/proofreading skills Detail-oriented, thorough, and methodical Ability to create and follow timelines and conduct long-range planning Ability to multi task performing numerous single or complex tasks without ignoring overall objectives Ability to judge when to initiate changes and make final determinations in the presentation of data in accordance with regulatory guidelines and reviewers' comments Ability to concentrate on the detail in a document without losing sight of the document as a whole At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. We offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees. Working Environment: PPD values the health and wellbeing 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.) PPD Defining Principles: - We have a strong will to win - We earn our customer's trust - We are game changers - 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.

About PPD: 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. About the Department: PPD Digital is PPD's solution to the growing digitalization and virtual trial requirements. PPD Digital offers flexible trial solutions across the digital spectrum to increase patient access and improve the patient experience, resulting in time efficiencies and data quality enhancements. PPD Digital links PPD assets drawing upon our operational, patient centered research and regulatory expertise. We design the optimal flexible strategy to extend patient reach and enhance data collection utilizing PPD assets and industry-leading technology and healthcare organizations. Our solutions fit the trial to the patient, rather than the patient to the trial. We overcome the geographic barriers associated with the traditional brick-and-mortar site visit and reduce the patient burden through a compelling patient-centered experience integrated seamlessly into everyday life. About the Position: Come join our team as PPD Digital revolutionizes the patient and site experience! We have an exciting remote position open for a *Digital Implementation Manager.* This role directs the technical and operational aspects of the eCOA and digital enablement (DE) projects, to achieve the successful completion of eClinical software builds. We offer this role at 3 career levels (I, II or III) and are open to hiring at any level for this opening. About our Culture, Career Advancement and Benefits: At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. We offer continued career advancement opportunities, award winning training and benefits focused on the health and well-being of our employees. Job Description: * Works with major functional area leads to identify and evaluate fundamental issues on the project, interpret data on complex issues, makes sound business decisions and ensure solutions are implemented. * Works to ensure all project deliverables meet the customer's time/quality/cost expectations. Accountable for ensuring all project deliverables meet the customer/contract expectations, providing accurate hour forecasts, reviewing pass-through costs and ensuring timely invoicing * Coordinates activities of all functional departments (data management, clinical programmers, testers, global clinical supplies, etc.) and vendors (translation, technology, copyright holders, etc.) involved in the project. * Works with team and management to develop plans/guidelines and test scripts for project implementation using PPD tools. Monitors and analyzes project status to ensure successful completion of project parameters, milestones, timetables. Works with team to identify potential risks, develop contingency plans. * Acts as principal liaison between Sponsor and PPD by facilitating the flow of information between PPD and client. Provides Sponsor with timely project updates, project related fiscal information, ensures correct protocol interpretations, and obtains direction and feedback on implementing scope of work. * Works closely with finance and legal to manage all financial and contractual aspects of the study including establishing and recognizing financial milestones for invoice and subcontractor purposes, subcontracting with third-party service providers, approving subcontractor invoices, establishing proper accrual for investigator grants, assisting with negotiation of the investigator grants as needed and similar pass-throughs. * Works with the project team to establish appropriate controls to ensure that project resources and expenses are aligned with budgets. Works closely with Project Management Director to provide details for the development and negotiation of contract modifications, as needed. * Ensures that appropriate training needs are occurring for the team members as needed. The ideal candidate will have knowledge of the software development life cycle and clinical outcomes assessments (COAs) including the development, validation, translation and migration (paper to electronic) process. He/she will have the ability to independently scope eCOA implementation projects and develop project plans and software requirements documents. *LI-Remote *Qualifications:* 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 8+ years') or equivalent combination of education, training, & experience. Knowledge of clinical outcomes assessments (COAs) including the development, validation, translation and migration (paper to electronic) process. Ability to independently scope eCOA implementations projects and develop projects plans and software requirements documents Knowledge, Skills and Abilities: * Knowledge of the software development life cycle * Knowledge of the key principles of cross functional project management (Time, Quality, Cost). * Solid financial acumen. * Applies a range of negotiation techniques to achieve desired outcomes with evidence of commercial and organizational acumen. * Displays effective communication skills (listening, oral, written) and can communicate in English language (oral,written). * Sound interpersonal skills, is flexible and adapts to changing situations. * Has the ability to persuade, convince, and influence or impress others. * Is organized, proficient at multi-tasking with good attention to detail. * Able to delegate, effectively prioritizes own and workload of project team members. * Ability to effectively use automated systems and computerized applications such as Outlook, Excel, Word, etc. * Possesses cross cultural awareness and is able to adapt appropriately. * Has experience with leading, liaising and coordinating cross-functional project teams. * Has knowledge/understanding of clinical development guidelines and directives. Management Role: No management responsibility 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 minimal travel PPD Defining Principles: - We have a strong will to win - We earn our customer's trust - We are game changers - 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-TK1

PPD's mission is to improve health. It starts as an idea to cure. It becomes a life saved. All in-between, it's you! We know that meaningful results not only require the right approach, but also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our talented, bright and energetic teams. PPD's Project Management department is a global team organized by therapeutic area. We partner directly with our clients to deliver projects from study start-up through close-out activities. In Project Management, you will oversee the delivery of PPD groups collaborating to support our clients. In short, you are a crucial piece in earning the trust of our clients. We have a new vacancy for *Senior Project Manager* in our *General Medicine team focusing on the areas of Dermatology, Immunology, Gastrointestinal, Dermatology or Nephrology*. This role is permanent and can be office or fully home-based in any of our EMEA countries. As a Project Manager, you are responsible for the overall management and successful delivery of the clinical study from start-up through close-out activities. You often work globally, with multi-functional leads to anticipate problems, find solutions and deliver results. You lead the collaboration that shows our clients we are one team focused on our purpose, mission, and strategy. Responsibilities: This position is responsible for directing and leading the activities in the General Medicine therapeutic area within and accountable for the P&L of a specific projects. Develops and drives the specific and overall therapeutic area strategies to ensure optimum performance and achievement of annual plans and targets. Has overall responsibility for instigating and leading change initiatives within the therapeutic area and works with peers of General Medicine in the overall leadership of the Project Management group. *Qualifications:* * Education and Experience: * * Bachelor's degree or licensed certified health care training; * Demonstrated track record of success in clinical development (equivalent to 7 years) and in leading and developing professional staff in a project led environment; * In depth understanding and experience with budgeting, forecasting and resource management within the General Medicine area (in the key therapy areas listed above); * Experience using project management software; * Valid Passport, where appropriate; Or equivalent combination of education and experience that provides the individual with the required knowledge, skills and abilities. * Knowledge, Skills and Abilities: * * Knowledge of the key principles of cross functional project management (Time, Quality, Cost); * Solid financial acumen; * Applies a range of negotiation techniques to achieve desired outcomes with evidence of commercial and organizational acumen; * Displays effective communication skills (listening, oral, written) and can communicate in English language (oral, written); * Sound interpersonal skills, is flexible and adapts to changing situations; * Has the ability to persuade, convince, and influence or impress others; * Is organized, proficient at multi-tasking with good attention to detail; * Able to lead, motivate and coordinate teams. Coach/mentor team members as appropriate; * Able to delegate, effectively prioritizes own and workload of project team members; * Ability to effectively use automated systems and computerized applications such as Outlook, Excel, Word, etc.; * Possesses cross cultural awareness and is able to adapt appropriately; * Has an understanding and appreciation of clinical research/development, including medical and therapeutic areas, phases and medical terminology; Has knowledge/understanding of clinical development guidelines and Directives. Has experience with leading, liaising and coordinating cross-functional project teams; 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-MC2 #LI-Remote

About PPD: 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. About Department: PPD Digital is PPD's dedicated business unit responsible to accelerate decentralized trials via strategic consultancy and excellence in execution. We offer flexible trial solutions across the decentralized (DCT) spectrum to increase patient access and improve the patient experience, resulting in time efficiencies and data quality enhancements. PPD Digital applies solutions drawing upon our operational, patient centered research and regulatory expertise. We design the optimal flexible strategy to extend patient reach and enhance data collection utilizing PPD assets and industry-leading technology and healthcare organizations. Our solutions fit the trial to the patient, rather than the patient to the trial. We overcome the geographic barriers associated with the traditional brick-and-mortar site visit and reduce the patient burden through a compelling patient-centered experience integrated seamlessly into everyday life. We act as industry leaders whilst driving to bend the time cost curve for our clients. About the Position: The *Digital Testing Engineer* will function as subject matter expert for various types of testing methodologies required for the PPD Digital department. The Digital Testing Engineer will lead testing efforts in the various stages of technology implementation, including eCOA. About our Culture, Career Advancement and Benefits: At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. We offer continued career advancement opportunities, award winning training and benefits focused on the health and well-being of our employees. Job Description: Reviews technical requirements and provides analysis on testing approach and content for the technology being deployed in the project * Leads test planning, documentation, test execution, error reporting, analysis and error verification * Works with Digital group and business test groups to support quality and acceptance testing * Conducts regression testing as needed per our control guidelines * Attend design meetings to understand technology requirements to prepare for testing of solution * Support existing business applications and end user training and documentation * Contribute to internal process and system enhancements * Adherence to established software development life cycle methodology and internal controls governing Change Management *Qualifications:* Education and Experience: Bachelor's degree or equivalent and relevant formal academic / vocational qualification Previous experience with eCOA and other clinical trial technology solutions that provides the knowledge, skills, and abilities to perform the job (comparable to 2-5+ years for I level, 5-8 years' for Senior level, 8+ years' for Principal level). Knowledge, Skills and Abilities: * Experience with system testing and writing test documentation (including script writing) * Understanding of the testing processes and SDLC * System testing experience with digital technology including eCOA * Experience working with IT Developers on system enhancements and new functionalities * Confident self-starter * Organized and Detail Oriented * Excellent problem-solving skills * Ability to quickly learn new concepts and software is necessary * Strong written and oral communication skills * Ability to work independently as well as with a team to meet hard deadlines * Ability to organize and present information in clear and concise formats 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 minimal as-needed travel (under 0-10%) PPD Defining Principles: - We have a strong will to win - We earn our customer's trust - We are game changers - 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 would love to hear from you. #LI-TK1

At AstraZeneca, we make a difference every day by delivering life-changing medicines to millions of people globally. Creating a more agile and inclusive environment means building an inspiring culture where we celebrate innovative thinking. This means we are opening up new ways to work, ground-breaking methods and bringing excellent teams together. Above all, we are passionate about science and driven to always put patients first. Join us and be part of an exceptional place to work! We have an opportunity for a *Regulatory Affairs Director (RAD) - Emerging Markets *to join our team. Emerging Markets Regulatory Affairs (EMRA) drive innovative, international, regulatory and patient-centric strategies enabling simultaneous global access to our products. We have a three-pillar strategy in Emerging Markets: Expansion, Innovation and Partnership. You will provide strategic leadership and have an understanding of regulatory science across international regions. Your experience and knowledge of drug/biologic development processes and strategies will enable you to influence cross-functional discussions with product teams. A thorough understanding of international commercial factors is needed for success in this role. *Key accountabilities / responsibilities: * *Project Regulatory Strategy* * Development and implementation of innovative regulatory strategies designed to deliver a rapid approval. Strategy should reflect international requirements. * Develop, communicate and update the International section of the Regulatory Strategy Document for assigned products/projects. * Delivery of regulatory milestones including assessment of the probability of regulatory success together with risk and mitigation measures. * Lead the objective assessment of emerging data against aspirations and update leadership teams on project risks and mitigation activities. *Leadership* * Single point of contact and Regional Regulatory Affairs representative on Regional Product Teams (across the Emerging Markets) * Planning and creation of the International dossier * Build and implement an optimal regulatory strategy for product(s) ensuring International needs are incorporated into the Global Regulatory Strategy that in turn contributes to the Global Product Development Plan. * Ensure business needs are understood within the Global Regulatory Strategy Team; encourage regional commercial engagement with proposed regulatory strategies, risks and mitigation plans. * Ensure effective regulatory representation in partnership with appropriate technical experts at all health authority meetings and clear documentation of the discussion and agreements. * Coach, mentor and lead regulatory teams to ensure objectives are successfully delivered to time and quality. * Provide leadership in product in-license/due diligence review, product divestment and product withdrawal. * Proactively contribute across RAD community and Regulatory Excellence objectives and activities. *Regulatory Environment* * Partner with commercial teams to monitor changes in the regulatory environment; support and advise accordingly. * Collaborate with commercial colleagues to influence guidance within leading Health Authorities. *Essential Criteria:* * Bachelor's degree in a science related field * Previous experience with Major Health Authority interactions * Extensive knowledge of regulatory drug development including product approval/launch. * Broad background in pharmaceutical business and experience in several areas within regulatory affairs, e.g. Global, European, International, Marketing Company or experience at a health authority. * Leadership and program management experience. * Ability to think strategically and critically evaluate risks to regulatory activities within a complex, critical, high-profile development program. * Successful contribution to a major regulatory approval in the International Region * Commercial and cross-cultural awareness; can work independently with Commercial and Marketing Company colleagues from across the globe. * Must demonstrate competencies of: critical thinking, strategic influencing, innovation, initiative, leadership and proficiency with both written and verbal communications. *Location: Cambridge UK, other locations can be considered*

Senior/Principal SAS Programmer (PK/PD & NONMEM required) Location: Cambridge, UK, Gothenburg, Swed or Warsaw, Poland Competitive salary and benefits *Play a critical role in making our pipeline accessible to patients.* Do you have expertise in, and passion for, SAS Programming? Would you like to apply your skills to impact all phases of drug development and regulatory interactions, in a company that follows the science and turns ideas into life changing medicines? Then AstraZeneca might be the one for you! AstraZeneca is a global, innovation-driven BioPharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines for some of the world's most serious disease. But we're more than one of the world's leading pharmaceutical companies. Join the team unlocking the power of what science can do. We are working towards treating, preventing, modifying and even curing some of the world's most complex diseases. Here we have the potential to grow our pipeline and positively impact the lives of billions of patients around the world. We work on some of the most complex and interesting challenges. A fast-paced and agile team, we are empowered and trusted to innovate and experiment. With access to our extensive capabilities and comprehensive pipeline, you'll be involved in countless submissions and a wide range of engaging projects along the complete drug development process. This position focuses on all aspects of data preparation, programming, validation and diagnostics to support pharmacometric and clinical pharmacology analyses at the study level to influence critical decision making throughout all phases of drug development and regulatory interactions. This person will support data preparation for pharmacometric analyses (Population PK, modelling and simulation, model-based and mechanistic knowledge), clinical pharmacokinetic activities, quantitative systems pharmacology (QSP) modelling, drug disease modelling and exploring machine learning and artificial intelligence approaches. Works directly with the pharmacometricians and clinical pharmacology scientists providing data support. Implements and supports standards and a harmonized approach to programming. With support from the Principal Pharmacometrician and the TA lead, the incumbent will be responsible for integrating internal (and external) data to support interpretation and decision making at the study level and with some support at the project level. *Accountabilities* * Accountable for expert data integration, manipulation and preparation results at the study level * Collates, cleans and prepares data to support M&S to influence study designs and go/no go decisions and support development of (mechanistic) drug-disease models within a specific disease domain * Contribute to regulatory documents and interactions (written) * Contribute to internal initiatives to develop the pharmacometric discipline including its processes * Participation in peer review of ongoing activities, reports and presentations * Compliance with Good Clinical Practice (GCP) regulations as well as internal/external guidance's * Build infrastructure, software and standards using programming macros * Recommend tools, updates and upgrades * Occasional interactions with leaders as clinical experts * Engage with vendors on data delivery and technical issue and data transfers *Essential* * *Strong SAS programming skills* * *Demonstrated expertise in data preparation and programming to support pharmacometrics, including PK, PKPD and/or statistics* * BSc or post graduate qualification (or local equivalent) in Mathematics, Statistics, Informatics, Life or Social Sciences, or equivalent experience * Demonstrated data programming and clinical development expertise and experience exemplified by extensive years of drug development experience, with emphasis on data preparation of Clinical Pharmacometrics * Expert knowledge of data preparation and programming practices (CDISC, SDTM, ADaM) to support pharmacokinetics and Model-Based Drug Development *Desirable* * Varied programming languages (SAS, R, Python) * Knowledge of Browser programming skills (JSON, Java, Spring), * Experience in early and late stage drug development * Experience with relevant software and tools within the field of MBDD (e.g. SIMCYP, R, NONMEM, Monolix, Winbugs, Stan, Phoenix, PKS) (T) * Good knowledge of global regulatory, compliance, processes, standards and issues specific to clinical pharmacology * Quantitative/Scientific background (Statistics, Engineering, Biological Science) *Why AstraZeneca?* At AstraZeneca we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There's no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We're on an exciting journey to pioneer the future of healthcare. *So, what's next? * * Are you already imagining yourself joining our team? Good, because we can't wait to hear from you. * Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available and we hope it's yours. *Where can I find out more?* * Our Social Media, Follow AstraZeneca on LinkedIn []() * Follow AstraZeneca on Facebook []() * Follow AstraZeneca on Instagram []() Date advert opened: *7th April 2021* Date advert closed for applications: *7th March 2021*

We seek an individual with excellent organisational, interpersonal, IT and communication skills, all delivered with exceptional accuracy and a 'can do' attitude. You will be an individual with a sound understanding of both HR best practice and project delivery support, capable of prioritising workload to meet multiple deadlines...... click apply for full job details

Senior/Principal Regulatory Affairs Specialist 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. If you're a strategic thinker, planner and multitasker as comfortable working independently as you are on a team in delivering compliant deliverables based on solid judgment, PPD is the place to be. Our global regulatory experts contribute the regulatory strategy and knowledge to help our clients navigate the challenging regulatory environment - and help get life-changing therapies to patients faster. PPD is seeking a Regulatory Affairs Specialist to join our growing Regulatory Affairs department. This is a fantastic opportunity to further your regulatory career and develop your expertise in this field. In this role you will be a pivotal team member with ideally with regulatory experience. You will provide innovative solutions including global regulatory therapeutic area expertise and client interface to provide strategic regulatory intelligence, guidance and regulatory expertise for product development from preclinical through registration and product optimization. You will feel confident providing regulatory advice and carry out projects in the provision of regulatory affairs services whilst acting as liaison with internal and external clients in the provision and marketing of these services. You'll work with the Regulatory Affairs management to perform the day to day operational aspects of the department such as: preparation and assembly of global regulatory submissions unassisted, interacting with sponsors, review and assess clinical trial regulatory documents, review and assess scientific literature. You will also act as prime interface with the sponsors of assigned projects. The following skills are required to be successful in this position: • Experience developing regulatory strategies globally • Experience and knowledge of bid defence meetings • Experience leading global regulatory projects • Client facing experience *Qualifications:* What the role requires you to have: • Bachelor's degree or advanced degree preferred, or equivalent and relevant formal academic / vocational qualification • Previous experience that provides the knowledge, skills, and abilities to perform the job • Knowledge of the global clinical trials landscape • Proven project management experience, and experience performing effectively in a client facing role Knowledge, Skills and Abilities: • Excellent command of the English language (written and oral) 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; expert knowledge of ICH and other global regulatory guidelines • Excellent analytical, investigative and problem-solving skills • Understanding of budgeting and forecasting 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-SH1 As we are likely to receive many applications, sometimes we are unable to provide feedback to everyone.

*Programming Team Leader, Early Biometrics & Statistical Innovation (EB&SI)* *Location: Cambridge, UK* *Competitive salary and benefits* *Play a critical role in making our pipeline accessible to patients.* Do you have expertise in, and passion for, Statistical Programming? Would you like to apply your skills to impact all phases of drug development and regulatory interactions, in a company that follows the science and turns ideas into life changing medicines? Then AstraZeneca might be the one for you! AstraZeneca is a global, innovation-driven BioPharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines for some of the world's most serious disease. But we're more than one of the world's leading pharmaceutical companies. Join the team unlocking the power of what science can do. We are working towards treating, preventing, modifying and even curing some of the world's most complex diseases. Here we have the potential to grow our pipeline and positively impact the lives of billions of patients around the world. We work on some of the most complex and interesting challenges. A fast-paced and agile team, we are empowered and trusted to innovate and experiment. With access to our extensive capabilities and comprehensive pipeline, you'll be involved in countless submissions and a wide range of engaging projects along the complete drug development process. At AstraZeneca we're driving leading-edge approaches to drug development across many business areas - within Early Biometrics & Statistical Innovation (EB&SI) a data-centric focus is helping us work more efficiently and creatively to bring the right medicines to the right patients. Our biometrics teams use their expertise in statistics and programming to answer drug development objectives and reduce uncertainty in product development, driving better business decisions with quantitative reasoning. The Programming Team Leader sits within our Early Programming group in EB&SI, aligned either to Cardiovascular/ Renal/ Metabolism (CVRM) or Respiratory, Inflammation, and Autoimmunity (R&I), and is responsible for providing statistical programming expertise to support the design and interpretation of early clinical studies and development programmes. Working as part of Data Science and AI, you'll be able to access technology at the forefront of science in an innovative environment, where you will have scope to develop creative statistical ideas and approaches, and to apply them in your work. Welcome to Cambridge (UK), one of over 400 sites here at AstraZeneca, providing a collaborative environment where everyone feels comfortable and able to be themselves is at the core of AstraZeneca's priorities, it's important to us that you bring your full self to work every day. In this role, we will give you the chance to utilise your statistical programming expertise in analysis and reporting of clinical trial programs; submission and defence of regulatory filings and the generation of evidence to support product commercialisation and reimbursement. *Main duties and responsibilities* The Programming Team Leader provides leadership, line management and development to a team, offering programming expertise and mentoring. This includes effective management of initiatives to improve quality and integrity of information interpretation, as well as promotion of best practice and standards to enhance the value and contribution of programming across EB&SI. In addition to the above, the Programming Team Leader will be expected to influence and contribute to the development, sharing and support of new procedures, standards, tools, or techniques to improve quality, efficiency, and effectiveness across all areas of work. *Requirements* Essential * BSc or post graduate qualification (or local equivalent) in Mathematics, Statistics, Informatics, Computer Science, Life or Social Sciences * Excellent interpersonal skills * Genuine commitment to drive innovation and improve efficiency * Extensive SAS programming expertise. * Excellent Knowledge of Analysis and Reporting within Clinical Development * Comprehensive knowledge of technical and regulatory requirements related to the role * Experience of CDASH/SDTM/ADaM CDISC standards * Demonstrated communication skills Desirable * Line management/ leadership experience * SAS certification * Knowledge of other programming languages such as R or Python *Why AstraZeneca?* At AstraZeneca we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There's no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We're on an exciting journey to pioneer the future of healthcare. *So, what's next? * * Are you already imagining yourself joining our team? Good, because we can't wait to hear from you. * Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available and we hope it's yours. *Where can I find out more?* * Our Social Media, Follow AstraZeneca on LinkedIn []() * Follow AstraZeneca on Facebook []() * Follow AstraZeneca on Instagram []() *More information* For more information about these positions please contact Per Arne Stahl [](mailto:) Date advert opened: 9th April 2021 Date advert closed for applications: 9th May 2021

Bioinformatics Post-Doc- Pipeline Developer This is a great opportunity for a Bioinformatics/ Comp Bio/ Computer Engineering/ Data Science/ Statistical Genetics Post-Docs and PhD graduate to join the R&D Computational Biology group. This role will be placed within the newly formed pipeline team which oversees the development and maintenance of the company's production pipelines. The candidate will work closely with the bioinformatics, software development and system administration teams to develop new pipelines into robust and scalable products. The candidate will have strong communication skills, a delivery focused attitude and the ability to interface with different teams. This position offers the exciting opportunity to work at the frontier of liquid biopsy-based cancer diagnostics, seeking entire product development pipeline from concept, clinical validation, to commercial product. This role will involve applying a deep understanding of HPC to the analysis of NGS cancer genomics variant data and innovative algorithm design. We expect that applicants will have prior experience in the field of bioinformatics and a solid background in pipeline development and optimisation in relation to NGS analysis; for example, an MSc or PhD degree in a relevant field and/or industry experience. Key Responsibilities Include: *Develop new and scale existing algorithms and pipelines to production ready, regulatory compliant cancer diagnostics products *Interface between bioinformatics, software development and system administration teams to prioritise and organise work *Contribute to quality management of computational biology processes and development of systems that conform to regulatory standards Key Requirements Include: *Proven track record with HPC in context of biomedical data analysis (essential) *Experience with implementation and maintenance of NGS data analysis pipelines (essential) *Full working proficiency in Python and R (essential) *Full working proficiency in Linux system administration (essential) *Full working proficiency in relational databases, such as MySQL, PostgreSQL or Oracle (essential) *Full working proficiency in software versioning systems, e.g. git, svn (essential) *Knowledge of cancer genomics (desired) *Full working proficiency in a compiled language, preferably C or C++ (desired) *Experience with algorithm and systems design for parallel computing (desired) *Experience with Docker (desired) *Experience with AWS products, including EC2, Batch, S3, Lambda (desired) *Prior experience with work in a regulated environment, in particular for software and quality assurance, such as ISO 13485, EN 62304, ISO 15189, or other (desired) If you are interested in discussing this role further, then please send your CV to Sabrina Deo at Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities. By applying for this position you agree to our privacy policy which can be found here:

*Associate Director, Statistical Programming - Early Oncology* Location: Cambridge, UK or Warsaw, Poland Competitive salary and benefits Would you like to be a part of a Programming group, who has direct strategic impact on drug development, playing a key role in getting medicines to patients? At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person. You will work in the* Oncology Programming* department that oversees and delivers global programming aspects of clinical development, leads and maintains the end-to-end standards and analysis and manages reporting production tools and information infrastructure. Oncology is driven by speed. Here you will be backed by leadership and empowered at every level to prioritise and make bold moves. What you'll do The* Associate Director, Statistical Programming* is accountable for the management of Programming teams. You will provide significant input to the strategy of Programming. You will need to have strong leadership skills and have a consistent record of managing a global team. Essential for the role * BSc or post graduate qualification (or local equivalent) in Mathematics, Statistics, Informatics, Computer Science, Life or Social Sciences * Excellent interpersonal skills * Genuine commitment to drive innovation and improve efficiency * Thorough knowledge of the clinical development process from development, launch through life cycle management * Ability to influence strategically and persuade tactfully to obtain desired outcomes while maintaining effective, positive, organisational relationships * Thorough knowledge of industry trends * Experience successfully leading global teams * R&D mindset * Strategically Develops Function * Eye For Business and experience of influencing and controlling budgets * Expert stakeholder management skills on a functional Level As a team we are deeply committed to transforming the lives of patients living with cancer - with the ultimate aim of eliminating cancer as a cause of death. There's no better place to make an impact - here we are uniquely placed with the funding, the ambition and the bravery to make it happen. *Next Steps - Apply today!* To be considered for this exciting opportunity, please complete the full application on our website at your earliest convenience - it is the only way that our Recruiter and Hiring Manager can know that you feel well qualified for this opportunity. If you know someone who would be an excellent fit, please share this posting with them. *Where can I find out more?* * Follow AstraZeneca on LinkedIn []() * Follow us on Facebook []() * Follow us on Instagram []() Date advert open: 9th April 2021 Date advert closed for applications: 9th May 2021

* PPD is seeking a highly skilled Senior Director of Project Management with an expertise in Rare Diseases to join our growing team. This person will drive new business endeavors and help lead strategy and growth to this area of PPDs clinical development business. * * Summarized Purpose: * * Works effectively across multiple divisions to direct the delivery of projects within cost, time and quality requirements. * Works with leadership in all functional areas on the continuous development/improvement of business processes to support cross functional teams and to ensure that work is uniform, complete and managed appropriately. * Serves as a liaison with Business Development and Bids/Contracts for the client presentations and proposal development. * Assists in resource utilization, policy development, and implementation of goals. * This position may be responsible for directing and leading the activities of a therapeutic area within a Region and accountable for the P&L of a specific therapeutic area. * Develops and drives the specific and overall therapeutic area strategies to ensure optimum performance and achievement of annual plans and targets. * Has overall responsibility for instigating and leading change initiatives within the therapeutic area and works with peers of Therapeutic areas in the overall leadership of the Project Management group. * Essential Functions: * * Ensures the timely execution of clinical trials with a focus on quality deliverables for a segment of the business which may include an entire therapeutic group within a region. In those cases, develops and drives the specific and overall Therapeutic Area Strategies to ensure optimum performance and achievement of annual plans and targets. Facilitates hand-off meetings and kick-off meetings to identify potential risks and work with the project team to develop and communicate contingency plans. Ensures project risks and potential contingencies impacting time/quality/cost of deliverables are discussed with Senior Management through appropriate escalation pathways. Reviews and assesses project profitability through the identification of "out of scope" activity in a timely manner and supporting follow through on all aspects of contract modification. * Manages the overall budgeting activity of the groups - annual and long range forecast. * Accountable for the line management of project managers and senior project managers. Effectively recruits, inducts and retains staff. Provides ongoing coaching, feedback and training, addresses performance issues, responsible for formal performance appraisals, development plans and career coaching. Responsible for proposing salary and bonus recommendations and supporting recommendations with appropriate documentation. * Communicates with sponsor(s) regularly to obtain direction and feedback on implementing scope of work as well as performance to date. Identifies unusual or significant problems encountered during the course of a clinical trial and proposes strategies for preventing or correcting significant problems. * Assists in business development activities to obtain additional contracts by writing and reviewing proposals, making presentations to potential clients and representing the location/division at appropriate professional meetings and conferences. Fosters client relationships and supervise strategic sell initiative of the division. *Qualifications:* * Qualifications: * * Education and Experience: * * Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 10+ years) or equivalent and relevant combination of education, training, & experience. * 5+ years of management responsibility * Proven leadership skills Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions. *Knowledge, Skills and Abilities:* * Demonstrates strong leadership skills. * Strong financial acumen. * Excellent judgment and decision making skills. * Effective oral and written communication skills including the ability to communicate in English, both orally and in writing. * Excellent interpersonal skills and problem solving ability. * Effective organization and negotiation skills. * Expert knowledge of project management principles and application. * Possesses depth of knowledge and practical application of budgeting, forecasting and resource management. * A relationship builder who is able to work effectively in matrix organizations. * Has successfully led national/international cross functional teams. * Demonstrates cultural awareness and adapts appropriately. * Knowledge of regulatory guidelines and Directives. * Skilled in process improvement, especially as it applies to clinical trials, clinical development and project management. * Knowledge of medical therapeutic area and medical terminology. * Strong marketing and negotiation skills. * Computer skills *Management Role:* * Directs through lower management levels and / or highly skilled specialist employees who exercise significant latitude and independent judgment. * Often heads one or more departments or a large centralized staff function. * In some instances may be responsible for a functional area (as determined by executive management) and not have subordinate supervisors or employees. * May manage employees across multiple regions. #LI-REMOTE *LI-MC2

This global biopharmaceutical company is seeking Early Phase Regulatory Affairs Candidates to join them on a contract basis till the end of 2021. The occupier of this position will be responsible for preparing regulatory submissions for Respiratory/Inflammation investigational and commercial products, including the preparation of documentation supporting Clinical Trial Applications (CTAs) and amendments. The crux of the role will involve: * Preparing CTA documentation * Attending Clinical Study Management meetings and represent international Regulatory Function at cross functional submission/ study meetings * Coordinate the submission of clinical, non-clinical and safety regulatory documents in accordance with Regulatory Bodies. * Post licensing commitments and Market Authorisation * Ensure licensed product packaging and associated information is maintained in accordance with regulations as well as provide input on labelling Applicants for this role are expected to: * Have regulatory submission experience, including support of CTAs within Europe * Understanding of the EU Centralized procedure and EU regulatory requirements * Have experience facilitating effective impact and influence strategic planning * Communicate with excellent verbal and written skills * Have experience representing Regulatory Affairs with cross-functional teams. * Experience working with document management systems. * Life Sciences degree, e.g. Biology, pharmacy or medicine.

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. PPD's data analytics group delivers a new approach to risk surveillance and centralized statistical monitoring, combining the power of statistical and analytical tools with expertise from operationally experienced staff to monitor and manage clinical study data. Data analytics staff explores study data holistically to pinpoint meaningful signals, resulting in more efficient and effective issue resolution and a proactive approach to risk detection. Using this data-driven approach, PPD can address study problems or site performance quickly, directing remediation activities where needed and positioning on-site monitoring activity in a targeted approach. Data analytics is an integral part of PPD's risk-based monitoring (RBM) strategy and supports centralized monitoring efforts. Ongoing data assessments from our data analytics group allows to adapt monitoring plans dynamically so that CRAs can focus on the factors that have the greatest impact on data integrity and subject safety. Regardless of the percentage of source data verification (SDV), the data analytics group's centralized statistical monitoring approach identifies risk signals that may be difficult to detect through traditional review methods, such as on-site monitoring. Data analytics evaluates data within and across studies, sites, countries and regions. Our analytic approach provides insight into: * Data errors, deviations * Trends, outliers * Unusual variation (or lack of variation) * Potential data manipulation, fraud * Other systematic errors or data integrity issues. As a Dir Data Analytics, you'll provide operational and strategic leadership within the department for development and delivery of centralized monitoring and risk surveillance in support of clinical trials. At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. We offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees. Summarized Purpose: Provides operational and strategic leadership within the department for development and delivery of centralized monitoring and risk surveillance in support of clinical trials. Essential Functions: Manages staff/ lower level management, which may include interviewing and selection, job description preparation, professional development, goal setting, performance management, 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. Serves as key integration point with other functional departments for, development and revision of cross-functional processes, identification and communication of functional-level trending, representation to other departments (eg training, awareness, etc.), and representation in broad department or company-wide initiatives. Contributes to overall tactical and strategic planning initiatives including direction and scope for DA activities and deliverables; tools, process and staffing to deliver to scope. Develops and manages client and partner relationships from DA function. Oversees and ensures quality of communication at project and program level. Drives departmental growth by planning, implementing, overseeing administrative and organizational efforts (e.g. hiring, project finances, resourcing, etc.). *Qualifications:* Education and Experience: 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 enough for an individual to meet the requirements of the role. Knowledge, Skills and Abilities: Demonstrated expert industry and clinical-trial specific deep functional-specific knowledge Proven coaching, mentoring and teaching skills; demonstrated expertise in leading and motivating teams Proven analytical skills with ability to extract meaning from data and apply to solve real-world problems Excellent judgment and decision-making skills Proven situational awareness, enterprise thinking, collaboration and negotiation skills Leadership level communication and presentation skills; ability to represent department to senior levels of management and cross-departmental forums Working Environment: PPD values the health and wellbeing 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 and/or standing for typical working hours. Able to lift and move objects up to 25 pounds Able to work in non-traditional work environments. Able to use and learn standard office equipment and technology with proficiency. May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments. Able to perform successfully under pressure while prioritizing and handling multiple projects or activities. PPD Defining Principles: - 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. IndeedPPDUS IndeedPPDClin #PPDHP *LI-OD1

CK Group are recruiting for a Lead Data Manager to join a company in the pharmaceutical industry at their site based in Cambridge on a fixed term contract basis for a period of 6 to 9 months. * Salary:* Circa £65,000 per annum. *Lead Data Manager:* Your main duties will be to: * Manage and lead the design and build of clinical databases through data management partner for oncology programmes. * Review and sign-off of all clinical data management documentation, study database builds and validation checks. * Establish and maintain a data management plans. *Your Background:* * The ideal candidate for this role will have substantial experience in early oncology clinical trials (Phase I to II). * Experienced using industry-leading electronic data capture technologies. * Knowledge of Database build and management skills. * Knowledge of data protection and clinical trial regulations around data management. *Apply:* For more information or to apply for this Lead Data Manager position, please contact CK Group, quoting job ref 50350. It is essential that applicants hold entitlement to work in the UK.

Electricians wanted for a high end commercial project in Cambridge. All applicants must hold a current/valid JIB/ECS grade card & IPAF certification. This project starts immediately and is due for c... ..... click apply for full job details

We are offering an accomplished BMS Commissioning Engineer the opportunity to join an exciting large pharmaceutical project in Cambridge. This contact is being offered on an inside IR35 basis and will be paid on a PAYE rate of £31.60 per hour plus holiday pay of £3.81 an hour ( so total rate of £35.41). There are excellent overtime rates as well...... click apply for full job details

Individuals wishing to become dry liners do not need to have any formal qualifications or training, although if you do they are likely to be advantageous. Prospective dry liners should have good practical skills, be able to read diagrams and technical drawings and have a good level of fitness. Dry liners build internal walls in residential and commercial structures...... click apply for full job details