Latest Clinical Research Associate Jobs

Senior Director, Global Real-World Evidence & Health Outcomes Research Lead, RSV Vaccines

Leads the global real-world evidence and health outcomes research strategy for RSV vaccines, serving as the single accountable point for data generation plans across in-market and pre-launch assets. Oversees study design, execution, translation and dissemination while engaging HTA agencies, guideline groups and payer stakeholders to support access and value-based pricing. Combines line management of analytic staff with cross-functional leadership across clinical, commercial and market access teams.

GSK USA - Pennsylvania - Upper Providence €151,500 – €252,500 pa

Senior Product Owner – Content Generation & Collaboration

Leads digital products for structured, collaborative and increasingly automated authoring of evidence and regulatory content across clinical, CMC, safety, regulatory and publications. Owns the roadmap, backlog and value case, shaping technical trade-offs with architects and engineers while embedding GxP, data-integrity and AI-governance requirements. Also mentors other Product Owners and manages strategic technology suppliers.

GSK London

Hybrid

Senior Engineer, CSV Validation

Hands-on senior role owning the computerised-system lifecycle for GxP systems, from impact and supplier assessments through validation, release, operation and retirement. Authors and executes CSV documentation, performs data integrity and 21 CFR Part 11 assessments, manages change controls and CAPAs, and supports regulatory inspections as a CSV subject matter expert.

Autolus Stevenage

Hybrid

Senior Computational Biologist - Early Discovery Oncology

Integrates phenomics, transcriptomics, genomics and proteomics data to nominate and validate oncology targets and define precision oncology patient strategies. Partners cross-functionally with biologists, chemists, engineers and translational experts to build target data packages and pilot novel discovery methods, including agentic target packages and mechanism-of-action work.

Recursion New York, United States US$151,800 – US$220,660 pa

Hybrid

SERM Medical Director, Oncology

Provides medical and scientific leadership in pharmacovigilance and risk management for oncology assets in clinical development, interpreting safety data, detecting and escalating signals, and delivering evidence-based benefit-risk recommendations. Represents Safety on cross-functional clinical matrix teams and Safety Review Teams, and presents to senior governance committees and regulators. Hybrid role based in the UK, Belgium, Poland or Italy.

GSK Wavre, Belgium

Hybrid

SERM Medical Director, Oncology

Provides medical and scientific leadership for pharmacovigilance and risk management of oncology assets in clinical development, interpreting safety data, detecting and escalating signals, and delivering evidence-based benefit-risk recommendations. Represents Safety on cross-functional clinical matrix teams and governance committees, and may lead Safety Review Teams. The role is hybrid across the UK, Belgium, Poland or Italy, with on-site attendance for key meetings.

GSK Siena, Italy £81,750 – £136,250 pa

Hybrid

SERM Medical Director

Provides medical and scientific leadership for pharmacovigilance and risk management of oncology assets in clinical development, interpreting safety data, detecting signals and delivering benefit-risk recommendations. Represents Safety on cross-functional matrix teams and governance committees, and interacts with regulators. Hybrid UK-based role with mentoring and process-improvement duties.

GSK London

Hybrid

SERM Medical Director

Provides medical and scientific leadership for pharmacovigilance and risk management of oncology assets in clinical development, interpreting safety data, detecting signals and delivering benefit-risk recommendations. Represents Safety on cross-functional clinical matrix teams and governance committees, and may lead Safety Review Teams. Hybrid role based in the UK with global regulatory and partner interaction.

GSK Wavre, Belgium

Hybrid

Associate Director - Global Regulatory Affairs (Oncology Therapeutic Group)

Develops and executes global and regional regulatory strategies for oncology assets, ensuring optimal labelling and approvals while maintaining compliance. Partners with the Global Regulatory Lead and cross-functional teams to shape development plans and regulatory interactions across multiple regions, assessing regulatory intelligence and competitive landscape to inform decisions.

GSK Stevenage €98,250 – €163,750 pa

Hybrid

Process Engineer, Drug Substance Development

Practical laboratory-based role developing and scaling up pharmaceutical processes for small molecules and oligonucleotides, working alongside chemists and material scientists. Combines digital, data and analytics with process simulation and modelling, and provides global engineering support during tech transfer to pilot plants and manufacturing sites.

GSK Stevenage

Senior Principal - Oncology

Lead complex oncology projects, designing and interpreting scientific and clinical strategies while guiding cross-functional teams on technical and regulatory matters. The role combines hands-on project leadership with mentoring colleagues and driving new methodologies, in a hybrid setup spanning London and Upper Providence.

GSK London

Hybrid

Associate Director - Global Regulatory Affairs (Oncology Therapeutic Group)

Develops and executes global and regional regulatory strategies for oncology assets, ensuring optimal labelling and approvals while maintaining compliance. Partners with the Global Regulatory Lead and cross-functional teams to shape development plans and regulatory interactions across multiple regions, assessing regulatory intelligence and competitive landscape to inform decisions.

GSK London €98,250 – €163,750 pa

Hybrid

Associate Director - Global Regulatory Affairs (Oncology Therapeutic Group)

Develops and executes global and regional regulatory strategies for oncology assets, ensuring optimal labelling, approvals and lifecycle compliance. Partners with the Global Regulatory Lead, therapeutic area head and cross-functional teams to shape development plans and regulatory authority interactions across multiple regions, while driving process improvement and innovation.

GSK Baar Onyx €98,250 – €163,750 pa

Hybrid

Associate Director - Global Regulatory Affairs (Oncology Therapeutic Group)

Develops and executes global and regional regulatory strategies for oncology assets, ensuring optimal labelling, approvals and lifecycle compliance. Partners with the Global Regulatory Lead and cross-functional teams on submissions, health-authority interactions and regulatory intelligence across multiple regions. Hybrid role based in London, Stevenage, Baar or Wavre.

GSK Wavre, Belgium €98,250 – €163,750 pa

Hybrid

Senior Principal - Oncology

Lead complex oncology projects, designing and interpreting scientific and clinical strategies while collaborating with cross-functional teams and external partners. Provide expert guidance on scientific, technical and regulatory matters, drive innovation in methodologies, and mentor colleagues. Hybrid role split between London and Upper Providence, Pennsylvania.

GSK USA - Pennsylvania - Upper Providence

Hybrid