Latest clinical research associate Jobs

Small Molecule CMC Leader - Senior Director

Lead CMC strategy and execution for small molecule drug development from Phase 2 through commercialization, managing cross-functional teams and global regulatory filings. Oversee tech transfer, process scale-up, and lifecycle planning while ensuring compliance with US, EU, and international standards. Interface with senior leaders and health authorities to drive successful product launches and post-approval activities.

GSK

Hybrid Permanent

SERM Scientific Director

The SERM Scientific Director will lead the safety evaluation and risk management of GSK's key assets, ensuring scientifically sound review and interpretation of data. They will develop and execute safety strategies, manage safety governance, and represent GSK on cross-functional teams to address product safety issues and improve regulatory adherence.

GSK

On-site Permanent

SERM Medical Director

The SERM Medical Director at GSK leads the safety evaluation and risk management of oncology assets in clinical development. Key responsibilities include interpreting safety data, managing safety signals, and providing expert medical input to support benefit-risk decisions. This role involves leading cross-functional teams, collaborating with regulatory authorities, and shaping the safety strategy for innovative oncology medicines.

GSK

On-site Permanent

Vice President, Medical Affairs

As Vice President, Medical Affairs, you will lead the development and execution of integrated medical strategies for Recursion's clinical portfolio, focusing on areas like oncology, rare diseases, and immunology. You will collaborate with cross-functional teams to build evidence, engage key stakeholders, and ensure the translation of scientific insights into meaningful patient impact.

Recursion North Tyneside, NE29 8EP, United Kingdom

On-site Permanent

Vice President, Real World Evidence (RWE)

Your work will change lives. Including your own.The Impact You’ll Make:Recursion is currently seeking a seasoned leader to join our team as Vice President, Real World Experience. This role will lead RWE generation across the Recursion portfolio. The role will...

Recursion United Kingdom

Biomedical Scientist (BMS)

The Biomedical Scientist (BMS) role involves performing analytical testing, operating and maintaining laboratory equipment, and processing patient samples in Blood Sciences disciplines. Responsibilities include result authorisation, quality assurance, and supporting patient care through collaboration with clinical and laboratory teams.

Acorn by Synergie Milton Keynes, Buckinghamshire, United Kingdom £16 – £20 ph

On-site Temporary Shift-work

Specialist Biomedical Scientist - Microbiology

Job Title: Specialist Biomedical Scientist - MicrobiologyLocation: BasildonSalary: £39,959 - £48,117 per annum + £10,000 Joining Bonus and wellbeing allowanceJob Type: Full Time, PermanentWe are expanding and are looking for an experienced Specialist Biomedical Scientist (BMS) who is ready to...

Synlab Basildon, Essex, United Kingdom £39,959 – £48,117 pa

Biomedical Engineer

This role involves the decontamination, inspection, repair, calibration, and reintegration of medical devices primarily from an Essex-based workshop, with occasional travel to customer sites. The engineer will conduct OEM training and deliver it to field teams, both remotely and in person, while also providing technical support and coordinating with clinical users and logistics teams. The position requires strong troubleshooting skills and the ability to explain technical concepts clearly to non-specialists.

FIELD Little Parndon, Essex, CM20 1PU, United Kingdom £35,000 – £38,000 pa

Hybrid Permanent

Biomedical Scientist

This role involves performing analytical testing and validation of patient samples in a clinical pathology laboratory, ensuring accurate and timely results for clinical decision-making. The scientist will operate and maintain laboratory equipment, adhere to strict quality standards like ISO 15189 and UKAS, and collaborate with healthcare professionals to support patient care. It offers career development within a regulated, team-oriented laboratory environment.

Acorn by Synergie St. Helier, London, SM5 1BZ, United Kingdom £31,049 – £46,580 pa

On-site Temporary

Key Account Manager

This role involves managing key accounts in the rheumatology sector across Scotland, focusing on building deep, value-driven relationships with healthcare professionals and stakeholders. The Key Account Manager drives sales growth through data-informed strategies, personalized customer engagement, and cross-functional collaboration, while ensuring compliance and ethical standards. The position emphasizes understanding customer needs, delivering tailored solutions, and translating insights into actionable plans to improve patient outcomes.

Novartis Derby, DE22 3FJ, United Kingdom

Permanent

Global Program Regulatory Manager - Neuroscience

This role involves driving regulatory strategy and execution for neuroscience products across global markets, with a focus on preparing high-quality submissions and managing interactions with health authorities. The manager will coordinate clinical trial applications, support approvals, and ensure compliance throughout the product lifecycle. Collaboration with cross-functional teams is essential to translate scientific data into regulatory outcomes.

Novartis London, United Kingdom

Hybrid Permanent

Associate Director, Statistical Programming

This role leads statistical programming efforts across global clinical trials, managing teams and driving innovation in data analysis and visualization. The individual will shape programming strategy, ensure audit readiness, and collaborate with cross-functional teams to deliver high-quality statistical outputs. Emphasis is placed on adopting modern tools like R, Shiny, and Git for reproducible, standardized workflows in drug development.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Regulatory Affairs Specialist

This role involves preparing and managing regulatory submissions for medical devices, ensuring compliance with EU MDR and ISO 13485 standards. The specialist will maintain technical documentation, support clinical evaluations, and collaborate with cross-functional teams throughout the product lifecycle. A key focus is staying current with global regulatory changes and ensuring continuous market access through timely renewals and post-market surveillance.

SRG Perivale, London, UB6 8DD, United Kingdom £50,000 – £60,000 pa

On-site Permanent

Regulatory Affairs Manager

Cure Talent are delighted to be partnered with a global medical device organisation recognised as one of the most established and successful healthcare companies in the world. With a diverse international footprint and a strong pipeline of innovation, the business...

Cure Talent Curbridge, Oxfordshire, Oxfordshire, United Kingdom £85,000 – £95,000 pa

Global Program Regulatory Manager - Neuroscience

This role involves driving regulatory strategy and execution for neuroscience products across global markets, with a focus on preparing and submitting clinical trial applications, managing health authority interactions, and ensuring compliance throughout the product lifecycle. The manager will work cross-functionally to translate scientific data into regulatory submissions and support timely approvals. It is a hybrid role based in London, requiring strong expertise in pharmaceutical regulatory affairs.

Novartis

Hybrid Permanent