Latest Pharmaceuticals Jobs

Scientist, Genetic Assays

This role involves designing and executing biochemical and molecular biology assays to support pharmacokinetic/pharmacodynamic analysis. Responsibilities include developing robust mRNA-based bioanalytical capabilities, troubleshooting scientific issues, and collaborating with external partners. The position also offers opportunities to work with Generative AI and digital tools to enhance scientific workflows.

Moderna Oxford, United Kingdom

Scientist, Genetic Assays

This role involves developing and executing biochemical and molecular biology assays to support pharmacokinetic/pharmacodynamic analysis. Responsibilities include assay development, data analysis, and collaboration with external partners, while staying current with scientific literature and regulatory guidelines.

Moderna

Senior Manager - CMC RA Biopharm Development Projects

This role involves leading global CMC regulatory strategies for biopharmaceutical development projects, preparing regulatory submissions, and advising on manufacturing and quality risks. You will collaborate with cross-functional teams and interact with regulators to ensure timely submissions and supply continuity.

GSK Canterbury, United Kingdom

Vice President - Oncology Clinical Development, Disease Area Head- Hematology

This role involves leading the clinical development strategy for GSK's Hematology portfolio, from early-phase studies to market launch. Responsibilities include shaping scientific and clinical strategies, managing cross-functional teams, and ensuring regulatory compliance and market readiness for innovative oncology therapies.

GSK Stevenage, United Kingdom

VP, Medicine Development Leader - Respiratory

Leads global development of a respiratory medicine from proof of concept to approval, serving as the single point of accountability. Builds and leads a cross-functional matrix team, drives strategic planning, regulatory engagement, and lifecycle management. Interfaces with senior leadership and external stakeholders to deliver evidence-based development plans and ensure optimal resourcing and execution.

GSK Stevenage, United Kingdom US$309,750 – US$516,250 pa

Hybrid Permanent

Senior Manager - CMC RA Biopharm Development Projects

This role involves leading global CMC regulatory strategies for biopharmaceutical development projects, preparing regulatory submissions, and advising on manufacturing and quality risks. You will work in cross-functional teams, interact with regulators, and mentor colleagues.

GSK United States

Senior Manager - CMC RA Biopharm Development Projects

This role involves leading global CMC regulatory strategies for biopharmaceutical development projects, preparing regulatory submissions, and advising on manufacturing and quality risks. You will work in cross-functional teams, represent CMC in regulatory interactions, and mentor colleagues.

GSK

VP, Medicine Development Leader - Respiratory

Lead the global development of a respiratory medicine from proof of concept to approval, serving as the single point of accountability. You will build and lead a cross-functional matrix team, define strategic direction, make evidence-based go/no-go decisions, and ensure alignment with GSK’s R&D and commercial strategies. The role involves close collaboration with regulatory, medical, manufacturing, and commercial stakeholders to deliver differentiated medicines and support lifecycle management.

GSK US$309,750 – US$516,250 pa

Hybrid Permanent

SERM Medical Director

This role involves leading pharmacovigilance and risk management strategy for GSK’s global pharmaceutical assets, with a focus on patient safety across clinical development and post-marketing phases. The Medical Director will lead safety governance, drive signal detection and risk mitigation, and represent GSK in regulatory discussions. It requires deep expertise in drug safety, cross-functional leadership in a matrix environment, and strategic input into global safety operations.

GSK United Kingdom

On-site Permanent

Medical Director-Oncology Clinical Development - GI

This role involves leading medical oversight in gastrointestinal (GI) oncology clinical development, ensuring patient safety and clinical integrity across study design, execution, and data interpretation. The Medical Director collaborates with cross-functional teams to integrate physician insights into clinical trials, engages with external experts and regulators, and contributes to regulatory submissions and scientific communications. The position requires deep expertise in oncology and clinical development within a global pharmaceutical environment.

GSK United Kingdom £222,750 – £371,250 pa

Medical Director-Oncology Clinical Development - GI

This role involves serving as the physician lead within an oncology clinical development team, providing medical expertise in study design, safety oversight, and data interpretation for gastrointestinal (GI) cancer trials. The Medical Director ensures patient safety and clinical integrity across clinical studies, collaborates with cross-functional teams and external experts, and contributes to regulatory submissions and scientific communications. The position supports GSK’s mission to advance innovative cancer treatments grounded in disease biology and real-world impact.

GSK £222,750 – £371,250 pa

Medical Director-Oncology Clinical Development - GI

This role involves leading medical monitoring and safety oversight for gastrointestinal (GI) oncology clinical trials, ensuring patient safety and clinical integrity. The Medical Director provides physician-level input into study design, data interpretation, and regulatory interactions, working closely with cross-functional teams and external experts. It emphasizes integration of medical expertise across clinical development, with a focus on advancing cancer treatments through innovative science and collaboration.

GSK £222,750 – £371,250 pa

Senior Manager - CMC RA Biopharm Development Projects

This role involves leading global CMC regulatory strategies for biopharmaceutical development projects, preparing regulatory submissions, and advising on manufacturing and quality risks. You will collaborate with cross-functional teams and interact with regulators to ensure timely and high-quality submissions.

GSK

Medical Director-Oncology Clinical Development - GI

This role involves leading medical monitoring and safety oversight for gastrointestinal (GI) oncology clinical trials within GSK’s global development programme. The Medical Director provides physician-level expertise in study design, data interpretation, and regulatory engagement, ensuring patient safety and clinical integrity across phases I–III. Working within a cross-functional matrix team, the role integrates medical insight into clinical strategy and collaborates with external experts and investigators to advance innovative cancer therapies.

GSK

Hybrid Permanent

Vice President - Oncology Clinical Development, Disease Area Head- Hematology

This role involves leading the clinical development strategy for GSK's hematology portfolio, from early-phase studies to market launch. Responsibilities include shaping scientific approaches, managing cross-functional teams, and ensuring regulatory compliance. The role requires deep expertise in hematology/oncology and a proven track record in clinical trial design and execution.

GSK United States

Hybrid Permanent