Latest Pharmaceutical Scientist Jobs

Director, Clinical Science – Oncology Clinical Development

Provides scientific leadership in oncology clinical development, contributing to study design, data interpretation, and regulatory documentation within a defined clinical programme. Works closely with cross-functional teams to ensure scientific rigor and alignment with clinical strategy, while supporting the execution of clinical studies from early to late stages. Focuses on generating robust clinical insights to advance cancer therapies with high unmet need.

GSK United States £189,750 – £316,250 pa

Hybrid Permanent

Director, Clinical Science – Oncology Clinical Development

Lead scientific strategy for oncology clinical studies, contributing to protocol design, data interpretation, and regulatory documentation within a global matrix team. Focus on advancing cancer therapies with high unmet need through rigorous clinical development and cross-functional collaboration. Emphasis on scientific excellence, real-world impact, and innovation in patient-focused drug development.

GSK PLN 472,500 – PLN 787,500 pa

Hybrid Permanent

Senior Audit Lead (EMEA GMP Audit)

This role involves leading and conducting GMP and compliance audits across GSK’s EMEA global supply chain, including internal and external manufacturing sites, R&D, and logistics providers. The Senior Audit Lead will assess quality, compliance, and technical risks in sterile, biopharm, and vaccines manufacturing environments, deliver clear audit reports, and support senior management with risk mitigation. The position requires subject matter expertise in sterile manufacturing and strong engagement with high-level stakeholders across regulated markets.

GSK €78,750 – €131,250 pa

Senior Director / Director, Oncology Translational Medicine Project Manager

This role leads the planning and execution of translational medicine strategies for GSK’s antibody-drug conjugate (ADC) oncology portfolio. The Director will integrate biomarker and diagnostic development with clinical programs, manage cross-functional teams, and ensure operational readiness for key milestones. They will provide strategic project management oversight, drive governance reporting, and support regulatory compliance across global oncology projects.

GSK Stevenage, United Kingdom

Hybrid Permanent

Senior Director / Director, Oncology Translational Medicine Project Manager

Leads end-to-end project management for GSK’s antibody-drug conjugate (ADC) translational medicine portfolio, integrating biomarker and diagnostic strategies across clinical development. Coordinates cross-functional teams and external partners to drive execution, governance readiness, and regulatory compliance. Focuses on strategic planning, risk management, and insight-driven reporting to support R&D decision-making.

GSK United States

Hybrid Permanent

Principal Medical Writer

The Principal Medical Writer will lead the creation of high-quality clinical and regulatory documents, working closely with cross-functional teams to ensure scientific rigor and clear communication. This role involves strategic planning, project management, and translating complex data into clear narratives, with a focus on regulatory compliance and process improvement.

GSK United States

On-site Permanent

Principal Medical Writer

Leads medical writing for complex clinical and regulatory projects, including protocols, study reports, and submission dossiers. Translates clinical data into clear scientific narratives and acts as a subject matter expert on regulatory standards. Works cross-functionally in a fast-paced, mission-driven HIV-focused environment.

GSK

On-site Permanent

Director Medical Writing Asset Lead

Lead medical writing strategy for one or more assets, primarily in Hepatology, across clinical development stages. Design and deliver high-quality clinical documents for global regulatory submissions, lead cross-functional teams, and drive process improvements using innovative technologies. This role involves shaping submission plans, mentoring teams, and influencing regulatory outcomes in a matrix environment.

GSK United Kingdom £119,250 – £198,750 pa

Director Medical Writing Asset Lead

Lead the medical writing strategy for one or more pharmaceutical assets, primarily in Hepatology, ensuring high-quality clinical documents for global regulatory submissions. Drive process improvements, mentor teams, and lead complex submission projects in a matrix environment. This role involves shaping document strategy, managing cross-functional collaboration, and applying regulatory expertise across the drug development lifecycle.

GSK €119,250 – €198,750 pa

Sr Director and Team Lead, Regulatory Labelling Strategy and Development, Oncology

Leads a global team responsible for developing and managing regulatory labelling strategies for oncology products across the drug development lifecycle. Ensures compliance with global regulations, collaborates with cross-functional stakeholders in R&D, safety, and commercial teams, and engages with regulatory authorities to shape innovative, patient-focused labelling. Plays a strategic role in governance and policy development within GSK’s oncology portfolio.

GSK £221,925 – £369,875 pa

Associate Director of Clinical Sciences

Lead clinical sciences strategy and execution for global oncology studies, with responsibility for end-to-end protocol development, clinical data review, and cross-functional collaboration. Focus on immuno-oncology with strong emphasis on regulatory compliance, patient safety, and scientific leadership across clinical development phases. Work within a matrix environment to guide study design, interpretation, and regulatory submissions.

GSK Stevenage, United Kingdom

Associate Director of Clinical Sciences

This role involves leading clinical sciences activities in global oncology studies, with responsibility for end-to-end protocol development, clinical data review, and cross-functional collaboration. The individual will shape study design, interpret results, and ensure regulatory compliance across phases of development, with a focus on immuno-oncology. The position requires scientific leadership, engagement with external experts, and contribution to regulatory submissions and clinical strategy.

GSK United States

Associate Director of Clinical Sciences

This role involves leading clinical sciences activities within global oncology R&D, focusing on study design, protocol development, and clinical data review across the development lifecycle. The individual will act as a subject matter expert, ensuring scientific rigor and regulatory compliance while collaborating with cross-functional teams and external partners. A key focus is on immuno-oncology, with responsibilities spanning from early-phase to late-stage clinical development.

GSK

Clinical Development Medical Director- Hepatology

Lead clinical development for hepatology assets, designing and executing translational and clinical studies to advance novel liver disease treatments. Provide medical oversight, shape development strategies, and collaborate across functions to deliver innovative medicines. Engage with regulators and external experts to drive proof-of-concept and lifecycle expansion opportunities.

GSK Stevenage, United Kingdom US$202,500 – US$371,250 pa

Hybrid Permanent

Medical Director Clinical Development- Aging

Lead clinical development for aging-related programs within GSK’s Respiratory, Immunology & Inflammation Research Unit. Provide clinical and scientific leadership across translational and clinical studies, design development plans, and guide regulatory strategy. Work cross-functionally to advance innovative medicines targeting underlying organ dysfunction and unmet medical needs in aging.

GSK Stevenage, United Kingdom US$189,750 – US$316,250 pa