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Excellent opportunity for a UK GMC registered physician looking to join a leading global pharmaceutical company. Based within the EU HQ you will contribute to the provision of a fist class Pharmacovigilance service by undertaking comprehensive medical evaluation of individual case safety reports (both spontaneous and clinical trial) and supporting the General Safety Officers (GSO) in aggregate report production.
Read More Fantastic opportunity for an experienced Medical Information Specialist looking to work within the European HQ of a global pharmaceutical organization. Acting as the therapy area expert within Oncology your will provide quality first line medical information service to the UK and Ireland and expert second line support for affiliates across Europe.
Read More An excellent opportunity to move into the pharmaceutical industry and develop your career in early clinical research in this fast growing and innovative company working on antivirals and vaccines.
Read More Leading Global Biopharma. We are looking for a Senior Medical Advisor to support their products in the Movement Disorder CNS area. Based in Berkshire – full time role.
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Norgine. Global role. We are seeking an experienced Clinical Development Physician. Managing two or three Clinical Project Managers, and working within a cross functional team, you will lead the medical direction and clinical strategy for the assigned projects.
Read More Opportunity for a Medical Information, Scientific Advisor or Medical Writer to move their career into Medical Editing. Our Client, a well established publishing and communications company is looking for a scientific expert to join as their Special Projects Editor within Diabetes. The role is broad and exciting and will see you not only researching and writing but also variations such as managing video shoots and events along the way.
Read More Opportunities for all levels of experienced Regulatory Affairs officers to join this specialist Pharmaceutical Company. The roles start at Officer level and move to Senior Officer. Responsibilities will include collating documents and preparing Marketing Authorisation Applications, to co-ordinating cross-functional teams to prepare responses to questions from authorities.
Read More A chance to step up to a man management role in this dynamic pharma company.
Read More A fantastic opportunity for a Regulatory Executive looking to work within a global pharmaceutical company. You will operate with some supervision (depending on experience) providing regulatory support to the UK and Ireland portfolio. Experience with post marketed products is essential.
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We are seeking to appoint a Pharmacovigilance and Medical Review Manager who will report directly to the Director of their local R&D structure. Covering the UK, the Pharmacovigilance and Medical Review Manager will assist in all aspects of local Medicinal Safety, in accordance with applicable regulatory requirements, guidelines, laws, and Servier quality standards and practices and in close contact with Global PV in France. The role also offers line management experience, with 2 direct reports.
Read More Supports Medical Writers and Regulatory Affairs authors to ensure data accuracy and formal quality in the documentation used in Clinical Studies and Regulatory Submissions.
Read More To provide support and high quality medical and technical information, both reactive and proactive, to external and internal customers. This information must be of a high standard and conform to all UK legal requirements and company guidelines and policies.
Read More An exciting opportunity – EU role supporting their launch activity in Hepatology. Excellent step up for a Medical Advisor. Specialty Pharmaceutical company with headquarters in the UK
Read More To join this respected Global CRO as a Senior Clinical Research Associate (SCRA). You’ll manage site responsibility for clinical studies and mentor junior CRAs. The role is supporting the Oncology team and will be concentrated with trials in the Midlands and the North. The role can based from the Client’s Greater London offices or field based either in the Midlands or the North (Manchester area).
Read More 9 month maternity contract. This secondment will offer the individual an opportunity to focus on the medical writing needed in late stage clinical development projects. The individual will gain exposure to and interact with members of global Clinical Project teams, including Clinical, Contract Research Organizations, Global Regulatory Affairs, Safety and Statistics colleagues.
Read More The Regulatory Executive is responsible for preparing high quality documentation; liaising with relevant departments to ensure regulatory requirements for submissions are met and to proactively communicate with regulatory authorities in order to expedite approval of these submissions.
Read More Rare opportunity for a Senior Project Manager/Programme Manager looking to progress into an Associate Director role within a top tier Pharma Company. This role will involve both strategic and scientific leadership for assigned studies and/or have overall Clinical Operations responsibility for a specified compound within the Neuroscience portfolio. May also have responsibility for direct reports, including hiring and development.
Read More Here is a great opportunity to combine your scientific knowledge and writing skills in an important role with one of the world's leading healthcare companies. You will be responsible for the project management and preparation of vital safety regulatory reports for innovative products and part of a global team driving the development of our clients rich pipeline of new products to make a difference to the health and wellbeing of people across the world.
Read More Opportunity to join a growing Compliance Consultancy at varying levels with the flexibility of working permanently, or on contract. Our Client has built a solid reputation for delivering strong compliance solutions and cultures through training and consultancy within the pharmaceutical industry and can offer a new direction to your Compliance career / experience.
Read More Opportunity to join a growing Compliance Consultancy at senior level. Our Client has built a solid reputation for delivering strong compliance solutions and cultures through training and consultancy within the pharmaceutical industry.
Read More Experienced Medical Information Scientist required to a busy department within a global Pharmaceutical organisation. This is a fixed term contract (expires Jan 2013) with the flexibility to work 3 - 4 days/week. Successful applicants will have experience as 2nd line support to European Affiliates, supporting European brand teams and handling first line enquiries from UK HCP’s.
Read More Senior Study Management of Phase II and Phase III Oncology studies according to ICH guidelines in support of the clinical strategies defined in the Integrated Development Plan (IDP) as they relate to European specific responsibilities. Support of Phase I trials may also be required. Office based from London HQ.
Read More Study Management of Phase II and Phase III Oncology studies according to ICH guidelines in support of the clinical strategies defined in the Integrated Development Plan (IDP) as they relate to European specific responsibilities. Support of Phase I trials may also be required. Office based from London HQ.
Read More Our client is looking for an immediately available PV Manager to take responsibility for Pharmacovigilance within the UK. As the PV Country Head (PVCH) you will direct, manage and improve all Pharmacovigilance activities within their diverse product portfolio according to the UK legislation and as devolved from Global Pharmacovigilance. A unique opportunity for a Physician/non-Physician with extensive PV management experience within the UK. Excellent rewards
Read More Responsible for the project management activities of this respected CRO based to the West of London. The remit is to ensure all Oncology sponsor trials are conducted to regulations, safely and to budget. This role will suit candidates looking to move into the challenge of complex and/or orphan indications in addition to working with Sponsors from Biotech and smaller Pharma Companies or start up ventures.
Read More Responsible for providing strategic regulatory advice to global cross functional teams on early and late phase clinical trials, with specific emphasis on trial design, set up and programme implementation. Further responsibility includes leading scientific advice interactions.
Read More Responsible for the regulatory lead for a marketed product licensed through the Centralised Procedure coupled with supporting the preparation of an MAA for a product currently in Phase III.
Read More Top 5 Pharma. We are seeking an experienced Clinical Development physician, ideally with expertise in virology to join this global R&D group and lead the Clinical Science Team for the area.
Read More Top 3 Pharmaceutical Company. We are looking for a Therapy Medical Director to join the UK Medical team to provide leadership to their Vaccines team (17 strong). This includes Medical Affairs and Clinical Research. You will have significant involvement with the R&D team and also work closely with the teams that lead European and Global strategy.
Read More This position is for a Medical Liaison Manager, which is a field based role, and will be covering a high profile, upcoming Cardio Metabolism portfolio in the South West of England and South Wales. This is a great opportunity for you to combine your scientific background, clinical expertise with your flair for communication and relationship building.
Read More An opportunity to build your career in Pharmaceutical business analysis and project support. You will work alongside a busy development team in an extremely innovative biopharmaceutical environment. This position will appeal to individuals keen to utilise their Project Management qualification ie: PMP, CAPM, Prince 2
Read More To provide medical and scientific input to therapeutic European Brand Team, in order to optimise commercial efficiency both at product launch and throughout the product life-cycle. To act as a specialist resource providing a more detailed knowledge of medical information used to support key communication messages and to present medical communications data to KOLS on request. Answer medical information enquiries from European affiliates and assist with technical training.
Read More As PV Physician you’ll support medical activities for global Pharmacovigilance (PV) and risk management for products in Europe (EU) and other Global Research & Development EU territories. Permanent position office based in London within the EU Headquarters of this respected Global Pharma Company. Strong licensed and developing pipelines.
Read More As a Medical Science Liaison (MSL), you will act on behalf of the medical affairs department, establishing professional relationships with various stakeholders in Epilepsy. You will engage in the exchange of scientific data and sharing clinical information on a peer-to-peer basis. You are responsible for providing fair balanced, objective, scientific information and education to health care customers and to internal business partners as required by business needs.
Read More To coordinate, under supervisory direction, IMP packaging, labeling, distribution and accountability activities contributing to the on-time delivery of quality-driven clinical supplies. To collaborate with clinical supply team colleagues and external vendors in the creation of value within the overall clinical development process.
Read More Specialty Pharmaceutical company with headquarters in the UK. An exciting opportunity – broad role with real responsibility.
Read More The job holder must have a proven track record of operating in a compliance role within the Pharmaceutical industry, enabling them to demonstrate a thorough working knowledge of the ABPI Code. Experience of writing SOPs, developing and delivering training within own field of expert knowledge, formulating and implementing a compliance plan, whilst being able to develop and maintain strong working relationships across all functional areas, and at all levels, is essential.
Read More Exciting opportunity for an experienced regulatory specialist to join a global organisation offering excellent career progression. You will contributing to clinical development plans, global regulatory strategic plans and providing advice on EU regulatory clinical trial and marketing authorisation requirements to the International Project Teams or Regulatory Sub-team.
Read More This is an exciting opportunity for an experienced Medical Information / Medical Scientific Affairs specialist looking to further their career within Medical affairs. You will be responsible for handling UK Medical Information queries, ZINC review and providing product specific and SOP training internally and externally as required.
Read More Responsibility to design, implement and manage the quality systems for the control of manufacturing starting materials in line with the Global Quality and M&S strategy. You will manage a number of commercially critical, complex or large sized suppliers and be part of the quality team supporting Quality Material Management.
Read More Opportunity for a strong Clinical Program Manager to take ownership of a cross functional group and manage the ongoing development and strategy of programs and studies within this respected Global Pharmaceutical Company. Emphasis on pre-clinical / early phase / haematology and vendor management. Office based, permanent position offering high financial rewards.
Read More Excellent opportunity for a GMC registered medic with speciality training in clinical transplantation, nephrology or hepatology to step up to a European role to support products in the Transplantation area.
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Napp Pharmaceuticals – provide leadership to the 12 strong UK Medical Affairs team with this fast growing pharmaceutical company.
Read More Like many pharmaceutical companies our client in the UK faces some of the most challenging market access hurdles in the world. An opportunity has arisen to be part of the UK Market Access team ensuring access for key brands. Reporting to the Head of Health Outcomes you will play a pivotal role in the development of health outcomes strategy, driving health outcomes projects during the full life cycle of a product in order to maximize their competitive advantage.
Read More Fantastic opportunity for an experienced Regulatory Affairs specialist to take responsibility for management of Regulatory Affairs activities relating to one or more products. You will also be responsible for obtaining and maintaining the required regulatory approvals for those products, including clinical trial approvals and provide strategic regulatory advice to project teams in relation to product development (manufacturing, safety, non-clinical) and clinical development, Phase I through to licensure.
Read More Top 5 Pharma. We are seeking an experienced Clinical Development Physician with expertise in neuroscience, neurology, schizophrenia or psychiatry and Phase II/ III clinical trials to join this global team
Read More Working from home, the responsibilities of the International Audit and Compliance Manager include preparing annual audit plans, carrying out GXP audits of suppliers, CMOs and CROs, along with providing GXP training. You will also carry out self inspection of affiliates and internal departments, hosting GXP audits and training. The role does involve extensive international travel.
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Retroscreen Virology Ltd - An excellent opportunity to develop your career in early clinical research in this fast growing and innovative company working on antivirals and vaccines.
Read More Opportunity for a graduate with Pharmaceutical commercial analysis experience to provide interim commercial analysis support to the global commercial function of this exceptional pharmaceutical company. The interim Analyst will be responsible for generating regular standard commercial reports to support all Global Commercial activities. In addition, you will also provide analytical support to all Global Commercial activities, including business development evaluations and R&D projects.
Read More An excellent opportunity to develop your career in a role with international exposure and involvement with pharmaceutical OTC products and devices.
Read More An excellent opportunity to develop your career in an International role within this global pharmaceutical company. You will support one in-market product and prepare the launch activities for another within the Epilepsy area. Based at their new offices in Hertfordshire.
Read More Opportunity for a pre-clinical QA / Compliance professional to join the pre-clinical team with responsibilities for compliance and training of Non-Clinical Development (NCD) staff and to ensure Pharmaceutical Sciences, Biosciences, Exploratory and Discovery disciplines are compliant with the R&D and corporate policies and procedures. In addition, the Manager represents NCD dept. on SOP review committees, compliance and training meetings.
Read More An exciting opportunity for an experienced Scientific Affairs Manager looking for a strategic role with a European remit. Key responsibilities will include providing scientific and technical support to European medical affairs and marketing. You will play an integral role supporting and preparing the launch activities for key products, implement and manage sponsored Phase IV studies and data generation within European markets and coordinate affiliate generated data review and approval process. CNS / Neurology experience desirable.
Read More 9 month maternity contract. We are looking for a technically savvy Pharmacovigilance Scientist or Drug Safety Officer, who is looking to take on more responsibility in a global role. You will have case processing experience and be looking to develop further triage, review and global experience. Your technical expertise and interest in Electronic Reporting (user testing etc), will be prized in this role.
Read More Opportunity to join this Global Pharmaceutical Company as their permanent Senior GCP Auditor. Through the execution of quality audits, you’ll provide assurance of the level of GCP and GvP Compliance throughout the organization (Global).
Read More This is an excellent opportunity for an experienced Medical Liaison/late phase clinical trials expert looking for a challenging in-house role within a truly global organisation. Working with the European Medical Director you will play an integral role in providing medical scientific input into promotional materials within the Dermatology franchise.
Read More Opportunity for an experienced Regulatory Affairs Project Manager to join this well known and successful Pharmaceutical company. The role is offered on a permanent basis and can be based at either of the company’s sites, Hampshire or Berkshire. You will need experience of the UK market (MHRA), MRP / DCP and Variations and be happy deputizing for Senior colleagues.
Read More Opportunity for an experienced Regulatory Affairs Officer to join this well known and successful Pharmaceutical company. The role is offered on a permanent basis and can be based at either of the company’s sites, Hampshire or Berkshire. You will need experience of the UK market (MHRA), MRP / DCP and Variations.
Read More This is an excellent opportunity to use your ABPI Code Compliance skills to add value to a highly regarded Healthcare Compliance team. Your primary responsibility will be to advance the development, refinement and implementation of all ABPI Code Policies and Procedures as well as utilize your expert knowledge of the ABPI Code of Practice in order to advise, guide and investigate complaints.
Read More Exciting opportunity for an experienced Clinical Project Manager to manage operational clinical research aspects of a clinical study or studies (phase 2-3) within a European or global clinical development programme. Successful applicants will be immediately available and have experience managing European studies.
Read More Our Client is a top tier Pharmaceutical organisation looking for an experienced Statistical Manager to support the Biostatistics team by carrying out and overseeing programming activities of statistical programmers and external vendors to ensure timely and accurate programming and validation activities for clinical studies. As a senior member of the team, contributing to the overall efficiency and best practice running of the Biostatistics group, demonstrating the ability to work efficiently and to a high standard within a clinical team environment.
Read More Our client is a Top 5 Pharmaceutical company seeking an experienced Senior Medical Advisor to join their Clinical Development and Medical Affairs team. This particular role is in the Primary Care Franchise and will take on medical leadership responsibility for cardiovascular and metabolic products and key pipeline molecules currently in Phase III and IIIB studies which will be launched in the coming 2-5 years. This is one of those rare roles encompassing Medical Affairs and Clinical development.
Read More Permanent office based position for an experienced Regulatory Affairs Associate Director to join the team at this respected Global Pharmaceutical Company. The offices are based in Central London.
Read More Permanent position for a CMC Project Manager to work within this renowned Global Pharmaceutical Company. Responsibilities include: product registration, submissions, representing Regulatory cross functionally, coordinate affiliates and ensuring compliance across life cycle. The role has strategic elements and will see you mentor and train team members.
Read More Excellent opportunity for an experienced Medical Advisor to step up to a senior role with line management responsibility in this specialist independent pharmaceutical company. Based in state of the art offices in Cambridge.
Read More The Quality Manager position is new to this company and therefore you will not only be bringing your expertise to the company, but you will be an influential member of the management team from the outset.
Read More Top 5 Pharmaceutical company – experienced Medical Affairs Physician to be Medical Manager for the strong, growing pipeline of new products in the Psychiatry Franchise– specifically in schizophrenia.
Read More Our client is a top tier pharmaceutical organisation based in Hertfordshire. This is a unique role which will combine your knowledge of Clinical Operations, Drug Safety and implementing and managing process. You have strong leadership capabilities with the ability to provide direction for these processes through direct line management of the clinical operations CFU staff. You will have extensive experience working
Read More Opportunity for an experienced and responsible Regulatory professional to join this dedicated Reg Team to collate documents and prepare Marketing Authorisation Applications. You’ll also co-ordinate cross-functional teams to prepare responses to questions from authorities.
Read More Our client is a Top 5 Pharmaceutical company seeking to appoint an experienced Senior Medical Advisor to provide support for their products in the Haematology area. This is one of those rare roles encompassing Medical Affairs and Clinical development. The focus will be on a number of new product launches. Good industry experience to meet these challenges is more important than therapy background. Based at the company’s offices in Surrey.
Read More Top 5 Pharmaceutical company – experienced Medical Affairs Physician to be Medical Manager for the strong, growing pipeline of new products in the Inflammation Franchise. Based Hertfordshire
Read More Our Client is a top tier Pharmaceutical organisation looking for an experienced Medical Manager to cover a 12 month maternity cover within CVS. You will be responsible for their phase III CVS medicine, helping to steer the development and pre-launch activities.
Read More A 12month contract opportunity for a Clinical Science Manager (CSM) with main responsibility for the planning and clinical science data review/analysis for clinical trials. Reporting to the Clinical Science Director you’ll work closely with the Project Team and Service Providers to establish study protocol and ensure quality and risk management are consistent with the development plan.
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