Latest Clinical Research Associate Jobs

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

Accountable lead for real-world evidence and health outcomes research across RSV vaccine assets, both marketed and pre-launch. Drives data generation plan design, study execution, translation and dissemination, and engages external experts, HTA agencies and payer bodies to support access and value-based pricing. Sits on the Vaccines RWE leadership team, managing a portfolio of studies and matrix stakeholders.

GSK London €151,500 – €252,500 pa

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

Accountable lead for real-world evidence and health outcomes research across RSV vaccine assets, spanning in-market and pre-launch. Drives data generation plan design, study execution, translation and dissemination, and engages HTA agencies, NITAG bodies and payer stakeholders to support access and value-based pricing. Sits on the Vaccines RWE & Health Outcomes leadership team, managing a portfolio of studies and analytic staff.

GSK Wavre, Belgium €151,500 – €252,500 pa

Data Solution Architect

Designs end-to-end data solutions spanning data integration, data warehousing, master data management, governance and analytics for a biopharmaceutical company. Translates business requirements into data models, data flows and integration patterns, and leads architecture and design reviews across enterprise applications and cloud data platforms.

Autolus 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

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 benefit-risk recommendations. Represents Safety on cross-functional clinical matrix teams and governance committees, and interacts with regulatory authorities. Hybrid role based in the UK, Belgium, Poland or Italy.

GSK London

Hybrid

SERM Medical Director, Oncology

Provides medical and scientific leadership in safety evaluation and risk management for oncology assets in clinical development, interpreting safety data, escalating signals and delivering evidence-based benefit-risk recommendations. Leads Safety Review Teams and cross-functional matrix groups, representing Safety to governance committees and regulatory authorities. Hybrid role based in the UK, Belgium, Poland or Italy.

GSK Poznań, Poland £410,250 – £683,750 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

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