Latest regulatory affairs Jobs

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing expert Good Clinical Practice (GCP) compliance guidance to clinical trial teams, supporting decision-making on complex regulatory issues, leading quality issue resolution, and ensuring inspection readiness across global clinical programs. The manager will translate regulatory requirements into actionable insights, conduct self-assessments, and drive continuous improvement in compliance. Embedded within cross-functional teams, the role emphasizes proactive risk mitigation, data integrity, and collaboration with Quality Assurance and Development functions.

Novartis Ardross, Alba / Scotland, IV17 0YF, United Kingdom

Hybrid Permanent

Senior Clinical Trial Leader - Translational Medicine

This senior role involves leading the scientific and operational aspects of complex, global early phase clinical trials. Responsibilities include designing and delivering high-quality studies, leading cross-functional teams, and ensuring robust data for key portfolio decisions. The role requires strong scientific and leadership skills, with a focus on continuous improvement and team collaboration.

Novartis London, United Kingdom

Hybrid Permanent

Senior Principal Developer

This role involves developing and maintaining R packages and Shiny applications to support clinical trial data analysis and reporting. The developer will collaborate with statisticians and clinical teams to build automated, reproducible tools, while promoting open-source practices and responsible AI integration. Emphasis is placed on modernizing workflows through user-centric design, documentation, and deployment in production environments.

Novartis £57,050 – £105,950 pa

Remote Permanent

Forward Deployed AI Engineer

Forward Deployed AI EngineerThe opportunityWe are looking for a Forward Deployed AI Engineer to serve as the critical bridge between Latent Labs’ frontier generative models and the customers who rely on them. You will work directly with pharmaceutical and biotech...

Latent Labs London, United Kingdom, United Kingdom

Hybrid Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, including medical monitoring, data review, and safety assessments. The Medical Director will also contribute to protocol design, site selection, and investigator training, while mentoring others and ensuring data integrity and quality.

Pfizer United States

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to the study team. The position also involves mentoring others and contributing to strategic discussions with key stakeholders.

Pfizer

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and collaboration with internal and external stakeholders.

Pfizer

On-site Permanent

Clinical Development Medical Director (Associate Director)

The Clinical Development Medical Director (Associate Director) oversees medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and clinical support for studies, with potential mentorship and strategic input.

Pfizer

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to the study team and external stakeholders.

Pfizer

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and collaboration with internal and external stakeholders.

Pfizer

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and collaboration with internal and external stakeholders.

Pfizer

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to the study team and investigators.

Pfizer

On-site Permanent

Senior QA Specialist, Pharmaceutical Development Quality Assurance (Maternity Leave Cover / Home Based)

This role involves ensuring the quality and compliance of Investigational Medicinal Products (IMPs) developed and manufactured by contract partners. The Senior QA Specialist will lead batch reviews, manage product stability programs, conduct vendor audits, and maintain quality systems in line with cGMP standards. The position supports clinical trial supply readiness and regulatory compliance across the pharmaceutical development lifecycle.

Jazz Pharmaceuticals London, United Kingdom

Remote Contract

Head of Engineering & Product Development

Head of Engineering & Product DevelopmentLocation: Lancing, Sussex (onsite)Salary: Competitive + BenefitsAn exciting opportunity has arisen for an experienced engineering leader to take ownership of an R&D team within a growing organisation operating in the medical devices / highly regulated...

CBSbutler Holdings Limited trading as CBSbutler Lancing, West Sussex, United Kingdom

Maintenance Engineer

This role involves performing preventative maintenance, repairs, and safety checks on laboratory and manufacturing equipment to ensure reliable operation. The engineer will troubleshoot technical issues, support equipment installations with IQ/OQ/PQ validation, and maintain accurate records within a CMMS. They will also coordinate vendor activities and work with quality teams to uphold regulatory compliance in a highly regulated environment.

SRG Cambridge, Cambridgeshire, United Kingdom

On-site Permanent