Latest Life Sciences Jobs

Executive Director, External Strategy & Science Advocacy

This role involves leading the external engagement and policy advocacy for GSK's Development Sciences, working with regulatory bodies, industry consortia, and academic institutions to shape the future of pharmaceutical innovation. Key responsibilities include developing policy strategies, advancing technical capabilities, and building strategic partnerships.

GSK United States

On-site Permanent

Executive Director, External Strategy & Science Advocacy

This role involves leading the external engagement and policy advocacy for GSK's Development Sciences, working closely with regulatory agencies, industry consortia, and government bodies to shape the future of pharmaceutical innovation. The Executive Director will drive strategic partnerships, develop policy frameworks, and champion technical advancements in clinical development and data science.

GSK

On-site Permanent

Team / Research Leader (Translational Oncology), London

This role involves leading the development and execution of comprehensive translational strategies for Isomorphic Labs' oncology pipeline. You will collaborate with interdisciplinary teams, manage a group of biologists, and ensure the successful transition of AI-designed drugs from preclinical to clinical stages.

Isomorphic Labs United Kingdom

Hybrid Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

The Global Development Lead (GDL) in Internal Medicine is responsible for leading the clinical development of assigned assets, collaborating with cross-functional teams to design and execute clinical trials, and ensuring regulatory compliance. The role involves strategic planning, innovative thinking, and engagement with external stakeholders to drive the clinical development program.

Pfizer Manchester, M1 4HD, United Kingdom

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (MD)

The Global Development Lead (GDL) in Internal Medicine is responsible for leading the clinical development of assigned assets, collaborating with cross-functional teams to design and execute clinical trials, and ensuring regulatory compliance. The role involves strategic planning, regulatory submissions, and engagement with external stakeholders to drive the clinical development program.

Pfizer Manchester, M1 4HD, United Kingdom

On-site Permanent

Regional Regulatory Intelligence Manager

This role involves leading the regional regulatory intelligence strategy, ensuring alignment with global regulatory direction and Health Authority expectations. Responsibilities include identifying and translating regulatory intelligence into actionable insights, influencing regulatory outcomes, and driving cross-functional collaboration to embed intelligence into submission processes and templates.

GSK

Hybrid Permanent

Regional Regulatory Intelligence Manager

This role involves leading the regional regulatory intelligence strategy, ensuring alignment with global regulatory direction and Health Authority expectations. Responsibilities include identifying and translating regulatory intelligence into actionable insights, driving cross-functional collaboration, and supporting capability building and training.

GSK

Hybrid Permanent

Regional Regulatory Intelligence Manager

This role involves leading the regional regulatory intelligence strategy, ensuring alignment with global regulatory direction and Health Authority expectations. Responsibilities include identifying and translating regulatory intelligence into actionable insights, influencing regulatory outcomes, and driving cross-functional collaboration to embed intelligence into submission content and processes.

GSK

Hybrid Permanent

Regional Regulatory Manager

The Regional Regulatory Manager leads the development and execution of regional regulatory strategies for assigned assets, ensuring alignment with global goals and regional requirements. This role involves close collaboration with global and local teams, providing regulatory expertise, anticipating risks, and driving timely submissions and approvals.

GSK United Kingdom

Hybrid Permanent

Regional Regulatory Manager

The Regional Regulatory Manager leads the development and execution of regional regulatory strategies for assigned assets, ensuring alignment with global strategies and regional requirements. This role involves close collaboration with global and local teams to deliver timely, compliant regulatory submissions and approvals, while providing regulatory expertise and market insights to support decision-making and risk management.

GSK

Hybrid Permanent

Regional Regulatory Manager

The Regional Regulatory Manager leads the development and execution of regional regulatory strategies for assigned assets, ensuring alignment with global strategies and regional requirements. This role involves close collaboration with global and local teams, providing regulatory expertise, managing submissions and approvals, and driving cross-functional alignment to deliver best-in-class regulatory outcomes.

GSK

Hybrid Permanent

Regional Regulatory Manager

The Regional Regulatory Manager leads the development and execution of regional regulatory strategies for assigned assets, ensuring alignment with global strategies and regional requirements. This role involves close collaboration with global and local teams, providing regulatory expertise, managing submissions and approvals, and driving continuous improvement and innovation.

GSK

Hybrid Permanent

Protein Engineering and Innovation Scientist

This role involves leading the development and deployment of advanced in-silico protein engineering and design principles to generate complex reagents for drug discovery. You will collaborate with computational experts, protein expression teams, and external partners to design, generate, and test engineered proteins, contributing to scientific innovation and project delivery.

GSK Stevenage, United Kingdom

Hybrid Permanent

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of Biopharm, Vaccines, and Pharmaceutical facilities. You will evaluate compliance with GMP, policies, and regulatory requirements, and provide subject matter expertise on sterile manufacturing. The role requires strong communication and influencing skills, and involves travel to various sites across the network.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities across the EMEA region. You will evaluate compliance with GMP, regulatory requirements, and quality management systems, and provide subject matter expertise in sterile manufacturing. The role requires strong communication and influencing skills to engage with senior stakeholders and produce clear audit reports.

GSK Worthing, United Kingdom

Hybrid Permanent