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Our Client is one of the world's leading research-based pharmaceutical companies. This is an outstanding career opportunity for an experienced Senior CRA/Study Manager looking to progress into a Clinical Project Management role where you will be responsible for study milestones and deliverables within the Neuroscience group.
Read More Fantastic opportunity for a Medical Scientific Liaison / Medical Liaison / Scientific Advisor person looking to work within Nephrology, Transplants or Hematology. Previous experience in an Orphan or Ultra-Orphan environment a distinct advantage. This role will cover the UK and Ireland. PhD / PharmD or a relevant scientific degree essential
Read More A chance for an experienced Medical Affairs Physician to join this leading biotechnology company who specialise in rare diseases to support their portfolio in Haematology.
Read More IMMEDIATE or ASAP START - Our Client is one of the world's leading research-based pharmaceutical companies. This is an outstanding career opportunity for an experienced Clinical Project Manager looking to progress into an Associate Director level role with a Medical Affairs focus – the role will combine scientific input, operational expertise and a commercial overview of a leading product pipeline.
Read More Our Client is one of the world's leading research-based pharmaceutical companies. This is an outstanding career opportunity for Regulatory Affairs Manager looking to broaden their role within a truly global team. The successful applicant will have an in-depth knowledge of the EU Clinical Trials Directive and confidence and experience dealing with European Regulatory Authorities
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 Global Pharmaceutical Company with EU Headquarters based in Central London. Opportunity for an experienced EU Lead CRA / Study Manager to join on a 12month fixed term contract at EU Study Manager level. The roles are office based, five days a week.
Read More Global Pharmaceutical Company with EU Headquarters based in Central London. Opportunity, due to growth, for three 12month fixed term contracts at EU Study Manager level. The roles are office based, five days a week.
Read More Excellent opportunity for a CRA to gain global exposure within a top 5 pharmaceutical organisation. Applicants must live within a 10 mile radius of the Salford area and have at least 1 years’ experience working as a CRA in the UK. Respiratory experience would be an advantage. Daily rate circa £250/day for Ltd company contractors. PAYE salary also an option."
Read More Top 5 Pharmaceutical company – experienced Medical Affairs professional to be Medical Manager for the strong, growing pipeline of new products in the Virology Franchise. 12 month contract
Read More Opportunity to join this specialist medical systems company in this brand new role, as Quality and Regulatory Affairs Manager.
Read More Short term (2 - 3 month) contract within Top 5 Pharma South West London. Flexibility to work 3 - 4 days/week for an experienced Scientific Advisor. This is a key role requiring solid Scientific Affairs experience - ideally with vaccines experience
Read More The Associate, Commercial Regulatory Affairs will provide resource and support to the submission and implementation of new or revised Summary of Product Characteristics, Patient Information Leaflets and associated packaging (collectively referred to as Regulatory Product Information (RPI)) for approved products. Working closely with Managers and Senior Managers in Regulatory Affairs and the wider team, this is an excellent opportunity for a Regulatory Affairs Associate to gain experience in Global Pharma.
Read More Pharmacovigilance Physician to work for this leading biopharmaceutical company at European level. Would suit experienced candidates seeking international exposure or those seeking more autonomy.
Read More Experienced Medical Information Scientist required to a busy department within a global Pharmaceutical organisation. This is a 12 month fixed term contract with the flexibility to work 3 - 4 days/week or full time. 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 This is an excellent opportunity for either a Pharmacist with medicines information experience or for current Medical Information professional to join a top pharmaceutical company in this diverse and progressive Medical Information department. Based in Berkshire this is a full time position with excellent career progression.
Read More Great opportunity for an experienced Regulatory Affairs Consultant looking for 2 – 3 days/week over 6 months. You will have the ability to add immediate value within a busy Oncology team. Strong EU regulatory experience and a good understanding of US regulatory processes essential. Limited Company Contractors welcome to apply
Read More Rare opportunity to join a field based Medical position as a Medical Scientific Liaison with strong Head office project participation. Leadership potential will be a core component of this role as will be ABPI Code of Practice with a view to attaining medical signatory status for appropriate candidates. You will be an experienced field based Medical Science Liaison or PhD/Pharmacist with Neurology expertise. Experience within Epilepsy is an advantage. Field based with focus on the North of England with the head office located in the South East so the location is open.
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 An immediate need has arisen for an Associate Clinical Study Manager to sit within the International Centre for Therapeutic Research (ICTR). Ideally you will be B/MPharm or PhD qualified with 2 - 3 years’ experience working within clinical trials - ideally within phase I/II development. This is a rare opportunity to provide both operational and scientific support to the global clinical trial process.
Read More Really rather exciting opportunity for an experienced Programme Lead to be responsible for the management of a global clinical development programme to include oversight of vendors and the supervision and management of several Study Managers. It is a pivotal role as leader of the Clinical Program Team for a compound providing overall planning and execution of the clinical development plan.
Read More Top 5 Pharma. We are seeking an experienced Clinical Scientist with expertise in expertise in neuroscience, neurology, schizophrenia or psychiatry and Phase II/ III clinical trials to join this global team.
Read More 12 Month contract as Senior EU Clinical Compliance Specialist, office based in Central London. Ensuring EU clinical trial activity is conducted to GCP and ICH standards. This position is responsible for technically complex audits and overseeing external vendors.
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 immediately available Regulatory Manager to cover a 6 month contract with a top tier Pharmaceutical company based in Dublin. You will be based in Ireland and have the proven ability to effectively manage Irish/European registration activities.
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 has two urgent vacancies within their Regulatory Affairs Department. You will be immediately available and able to take on responsibility for clinical trial submissions, scientific advice, and regulatory input into clinical and drug development plans. You will also manage MAA submissions for compounds allocated as well as assisting with new pipeline projects and late stage candidates brought in through in-licensing. 6 month contract – either 5 days or 3 days/week.
Read More As PV Physician you’ll support medical activities for global Pharmacovigilance (PV) and risk management for Oncology products in Europe (EU) and other Global Research & Development EU territories. Twelve month contract to be office based in London within the EU Headquarters of this respected Global Pharma Company. Strong licensed and developing pipelines.
Read More Our Client has an immediate requirement for a Senior CRA to support their busy Oncology Department. You will be a lead CRA with monitoring experience within the UK and at least one other European country. Experience of Oncology clinical trials and tools (such as RECIST and NCI-CTC) is expected.
Read More Opportunity for an experienced and responsible Pharmacovigilance professional to join this dedicated Team within this Leeds based Pharmaceutical Company.
Read More Excellent opportunity for experienced CRAs to join this mid-sized friendly CRO based to the West of London. There are opportunities for CRA / CRA II / Lead CRAs / Senior CRA within the organization. Candidates with Dutch, Italian or German language skills would be highly desirable.
Read More A Unique Clinical Science Opportunity in a new and growing franchise. We require an experienced Clinical Development physician – ideally with a background in the respiratory area.
Read More As Regulatory Affairs Manager you’ll be responsible for planning and managing all regulatory activity associated with a UK and Ireland product portfolio. This small Pharmaceutical Company offers a fantastic working environment and is based just West of London.
Read More Top 5 Pharma. We are seeking an experienced Clinical Scientist ideally with expertise in virology, to join the industry in this excellent opportunity within global drug development through clinical trials.
Read More This is an exciting opportunity for an experienced Medical Science Liaison looking for an opportunity to work within a growing Biotech working within serious and rare conditions. This is a new role in the team and will cover the whole of the UK alongside the other Medical Science Liaisons. It is an influential role where you will lead efforts in recognising, identifying and integrating KOL relationships as well as identifying opportunities for scientific growth and medical evidence.
Read More As Senior Pharmacovigilance Compliance Specialist, you’ll verify that the Pharmacovigilance (PV) activities for all IMPs and Marketed Products are conducted in compliance with Volume 9a and all applicable local and international regulatory requirements. You’ll also assure all audits of external vendors and internal PV systems meet quality standards.
Read More As Associate Director Regulatory Affairs, you’ll lead the Regulatory Development strategy for the EU on two Global Diabetes (Endocrinology) products. You’ll plan, manage and execute regulatory activities liaising with global regulatory leadership whilst ensuring regional regulatory therapeutic area strategic guidance is adhered to on development projects and marketed products, including a Top 10 global product.
Read More Top 3 Pharmaceutical Company. We are looking for an experienced Medical Affairs Specialist to lead the medical activities for hepatitis in Europe, Asia Pacific, Japan and Emerging Markets. Based in west London
Read More As a Business Compliance Director you will be responsible for planning and implementing the UK strategy across compliance for the UK business in line with the ABPI Code of Practice for the Pharmaceutical Industry, UK laws and regulations, the Standards of Business Conduct and Ethics and all other applicable procedural documents.
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Roche UK - This is an excellent opportunity to provide strategic leadership to the growing Medical Affairs team for the cardio metabolism area as the company prepares for a major launch within the Cardiovascular area. Reporting to the Medical Director, you will develop and deliver pre-launch education, identify and close data gaps and develop strong relationships with Key Opinion Leaders through your team.
Read More As Medical Director you’ll support largely Phase III developmental programs, both regionally and internationally, however, flexibility to include earlier or later stage development is required. Responsible for the oversight of signal detection and risk management activities for designated global/regional products, together with global safety lead responsibly. Role includes line management responsibilities for junior physicians and/or scientists.
Read More Top 3 Pharmaceutical Company. We are looking for an experienced Medical Affairs Physician to lead the medical activities for the immunology or hepatitis areas for Europe, Asia Pacific, Japan and Emerging Markets. Based in west London
Read More 12 month contract for a Clinical Category Manager to join this respected Central London Pharmaceutical Company. The role sits within the procurement division.
Read More As a true Scientific Clinical Leader, you’ll have full responsibility for strategic planning for a Urology clinical project. Writing and implementing the Development Plan, managing effective communication internally and with external organizations and developing KOL relations. A real opportunity to be a senior player in a small Global organization.
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 Top 3 Pharmaceutical Company. We are looking for a Senior Medical Advisor to join the UK Medical team to support their pipeline products in the oncology area and support launches in melanoma. You will have significant involvement with the R&D team and also work closely with the teams that lead European and Global strategy. Based in west London – full time role.
Read More Day to day responsibility for owning and driving compliance initiatives for the UK - articulating, designing and determining standards of compliance and ethical conduct to the organisation through the Company’s Code of Conduct and a series of company policies and procedures to ensure compliance.
Read More There is an opportunity for an experienced medical information specialist to join a friendly and dynamic Medical Information team within the Medical department of a global Pharmaceutical company. As a Therapy Area Advisor / Medical Information Specialist your primary role is to provide support for internal customers including the Brand, Medical, Training and Healthcare Management teams within the Oncology portfolio.
Read More To provide a quality first line medical information service to the UK and expert second line support for affiliates and Business Units in Europe. To operate as the UK Local Safety Officer
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Norgine. Global role. We are seeking two experienced Clinical Development Physicians - one for late stage programmes and one for early stage programmes. 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 Top 5 Pharma. We are seeking a physician with expertise in neuroscience, neurology, schizophrenia or psychiatry and Phase II/ III clinical trials to join this global team.
Read More Top 5 Pharma. We are seeking a physician with expertise in infectious disease, hepatology or possibly gastroenterology to join the industry in this excellent opportunity to use your clinical and medical expertise driving an international drug development through clinical trials
Read More Leading biopharmaceutical company This is an excellent opportunity for an experienced clinical development physician to support the development of one or more new chemical entities in the GI/ Hepatology areas from First in Man studies to pivotal Phase III studies through to regulatory submission.
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 Manage the Medical function for this Top 5 Pharma’s business in Ireland, based in Dublin. As well as sitting on the management team, there is broad line responsibility including a Medical Advisor, 2 CRAs, 2 Regulatory, 2 Pharmacovigilance Assessors, 2 Medical Information and an Administrator.
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 Top 5 Pharmaceutical company – experienced Medical Affairs Physician to be Medical Manager for the strong, growing pipeline of new products in the Virology Franchise. Based Hertfordshire
Read More Top 5 Pharmaceutical company – experienced Medical Affairs Physician to be Medical Manager for the strong, growing pipeline of new products in the Virology Franchise. 6 months contract. 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 Top 5 Pharmaceutical company – experienced Medical Affairs Physician to be Medical Manager for the strong, growing pipeline of new products in the neurology Franchise – specifically in schizophrenia. Based Hertfordshire
Read More Top 5 Pharmaceutical company - Medical Affairs Physician to be Senior Medical Manager and lead the CNS Medical Affairs team. Providing Medical Affairs support for key CNS products, including clinical research programme, and development of the life cycle plan. Also a member of the international team. Based Hertfordshire
Read More Top 5 Pharmaceutical company – experienced Medical Affairs Physician to be Medical Manager for the strong, growing pipeline of new products in their oncology Franchise. Based Hertfordshire.
Read More This is an exciting opportunity for an experienced Senior Clinical Project Manager with experience working phase IIIb – IV clinical trials and a strong commercial acumen. Reporting into Medical Affairs you will work in close collaboration with Associate Directors of Medical Affairs, Associate Brand Directors and other Members of the Brand Teams.
Read More This is initially a six month contract for a Regulatory Manager to be office based in Central London. As Regulatory Affairs Manager you’ll plan and manage activities including to compliance to Competent Authority regulations, communicating to CROs and ensure regulatory applications are prepared in accordance with company SOPs, GCP and other guidelines.
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.
Read More As Senior Regulatory Affairs Manager within this Global Pharma Company, your remit will be supporting strategy and operational implementation for the EU region. This will include; CP, DCP, MRP, supporting CTAs and completing life cycle management activities. Some line management responsibility may be given at this level.
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The Associate Director Regulatory Affairs, at Allergan, is responsible for strategic regulatory input into Global Development Plans and subsequent implementation, to ensure the registration of commercially successful products (Class IIb and Class 3 Medical Devices) in the EU and Emerging Markets Region. This role carries line management responsibility
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