Latest Outsourcing Jobs

Associate Director, Translational Medicine Expert, TM Clinical Pharmacology

This role involves leading and managing multiple First-in-Human and Clinical Pharmacology studies, ensuring medical and scientific excellence. You will provide expert input into study design, safety, and reporting, and collaborate with cross-functional teams to align on program objectives and optimize processes.

Novartis London, United Kingdom

On-site Permanent

Senior Clinical Project Manager

The Senior Clinical Project Manager will lead the execution of one or more clinical trials from start to finish, ensuring compliance with regulations and managing cross-functional teams. This role involves planning, budgeting, and overseeing global clinical trials, with a focus on early phase oncology studies.

Recursion United Kingdom £165,900 – £211,100 pa

Hybrid Permanent

Associate Director, Biostatistics (2)

The Associate Director, Biostatistics, leads the statistical contribution to clinical development programs, ensuring appropriate methodologies for study design, data analysis, and regulatory submissions. They collaborate with cross-functional teams, manage outsourcing operations, and represent Biostatistics in regulatory interactions.

CSL United Kingdom

On-site Permanent

Associate Director, Biostatistics (2)

The Associate Director, Biostatistics, leads the statistical contribution to clinical development programs, defining statistical strategies, ensuring appropriate methodologies, and collaborating with cross-functional teams. They also manage outsourcing operations, represent Biostatistics in regulatory interactions, and support innovation in clinical trial design and analysis.

CSL

On-site Permanent

Disease Area Lead - Hepatology, Renal and Cardiovascular diseases

Leads clinical operations strategy and delivery across Hepatology, Renal, and Cardiovascular disease portfolios within GSK’s R&D engine. Oversees end-to-end development from early phase through life-cycle management, driving operational excellence, team development, and cross-functional alignment. Champions data-driven decision-making, risk management, and innovation adoption to accelerate high-impact assets.

GSK Stevenage, United Kingdom US$242,550 – US$404,250 pa

Hybrid Permanent

Disease Area Lead - Hepatology, Renal and Cardiovascular diseases

Lead clinical operations strategy for Hepatology, Renal, and Cardiovascular disease portfolios, driving end-to-end delivery from early phase through life-cycle management. Oversee a matrix team, align operational execution with R&D goals, and champion data-driven decision-making and innovation in clinical development. Shape culture, manage risks, and ensure inspection readiness across global assets.

GSK Canterbury, United Kingdom US$242,550 – US$404,250 pa

On-site Permanent

Senior Scientist - Protein and Cell Sciences

In this laboratory-based role, you will design, express, purify, and characterize recombinant proteins to support biologics discovery and development. Your work will directly impact the evaluation of novel therapeutic modalities and inform clinical decisions, using modern computational tools and rigorous experimental methods.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Vice President, Head of Clinical Operations

This role involves leading the clinical operations strategy and execution across Recursion’s development portfolio, from study planning to study closeout. You will build and mentor a high-performing team, manage global trials, and ensure operational excellence in an AI-native TechBio company.

Recursion United Kingdom

On-site Permanent

Investigator Contracts Lead, Sr. Manager

Leads clinical trial site contract negotiations and budget management for global studies, overseeing agreements and amendments with investigator sites. Acts as a key point of contact for complex contracting strategies, collaborates with legal and finance teams, and mentors junior negotiators. Focuses on risk mitigation, timeline adherence, and process improvements in a remote, matrixed environment.

Pfizer London, SW7 2AP, United Kingdom

Remote Permanent

Pharmaceutical Regulatory Affairs Officer

This role involves managing regulatory submissions and product lifecycle compliance for pharmaceutical products, with a focus on packaging, labelling, and interactions with the MHRA. The candidate will coordinate eCTD submissions, support variations, and ensure change control processes are followed across cross-functional teams. It's a hands-on position offering impact in a regulated environment with hybrid working and a clear regulatory focus.

Evolve Selection Leicester, Leicestershire, United Kingdom £40,000 – £50,000 pa

Hybrid

Pharmaceutical/Healthcare Sustainability Lead

We are partnering with a leading organisation in the Pharmaceutical, Healthcare and Retail Eye Care market, to recruit an impactful Pharmaceutical/Healthcare Sustainability Lead who will shape and drive the company’s environmental strategy. In this role, you’ll work closely with senior...

Evolve Selection Birmingham, West Midlands (county), United Kingdom £55,000 – £60,000 pa

Investigator Contracts Lead, Sr. Manager

This role leads the negotiation and execution of clinical trial contracts with investigator sites globally, managing both contractual terms and site budgets. The Senior Manager oversees complex or high-priority studies, resolves escalations, and collaborates with Legal, Finance, and pCRO partners to ensure timely site activation. It involves shaping contracting strategies, mentoring junior staff, and driving process improvements in a remote, global environment.

Pfizer Poland

Remote Permanent

Trial Vendor Associate Director

The role involves managing all clinical vendor-related aspects of global clinical trials, including vendor service delivery, contract negotiations, cost control, and user-acceptance testing for eCOA and IRT systems. You will collaborate closely with the study team and ensure quality and service standards are maintained throughout the study lifecycle.

Novartis London, United Kingdom

Permanent

Associate Director, Biostatistics 2

The role involves leading the statistical aspects of clinical development programs, including study design, data analysis, and regulatory submissions. Responsibilities include collaborating with cross-functional teams, managing CROs, and representing Biostatistics in regulatory interactions.

Appcast Enterprise Maidenhead, SL6 1QB, United Kingdom

On-site Permanent