Latest Pharmaceuticals Jobs

Labelling Strategy and Development, Oncology Team Lead

This role involves leading a global labelling team for oncology products, shaping clear and compliant product labels that support patient care and regulatory success. The position requires strategic oversight of labelling development from early stages through lifecycle management, working closely with cross-functional teams and regulatory authorities to drive innovative, patient-focused solutions.

GSK

Hybrid Permanent

Labelling Strategy and Development, Oncology Team Lead

Leads a global team responsible for developing and managing oncology product labelling across the drug development lifecycle. This role shapes regulatory-compliant, patient-focused labels by collaborating with cross-functional stakeholders in R&D, Regulatory, Safety, and Commercial. It involves strategic decision-making, engagement with health authorities, and driving innovation in labelling standards to support GSK’s oncology portfolio.

GSK

Hybrid Permanent

Executive Regulatory Science & Strategy Director, Oncology

This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include coaching regional and global regulatory leads, partnering with directors on innovative regulatory strategies, and representing the Global Regulatory Affairs function in senior interactions and health authority meetings.

AstraZeneca

On-site Permanent

Executive Director, Strategy, Oncology R&D

This role involves crafting and driving the global Oncology R&D strategy, integrating clinical, scientific, and commercial insights to shape portfolio priorities. You will advise senior leadership, optimize investment decisions, and collaborate across functions to deliver high-impact strategic outcomes.

AstraZeneca United States

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

Clinical Development Medical Director (Associate Director)

This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, including medical monitoring, safety data review, and clinical data management. The Medical Director will also contribute to protocol design, site selection, and investigator training, while mentoring others and ensuring data integrity and quality.

Pfizer Manchester, M1 4HD, United Kingdom

On-site Permanent

ViiV Healthcare (GSK) Medical Director, ViiV R&D Physician Center of Excellence

This Medical Director role involves managing and overseeing Phase 1-4 clinical trials for ViiV Healthcare, focusing on the development of innovative HIV treatments. Key responsibilities include designing study protocols, ensuring medical governance, managing safety events, and collaborating with internal and external stakeholders to drive the success of clinical trials.

GSK

On-site Permanent

ViiV Healthcare (GSK) Medical Director, ViiV R&D Physician Center of Excellence

The Medical Director role at ViiV Healthcare focuses on managing and overseeing Phase 1-4 clinical trials, ensuring the successful planning, execution, and reporting of protocols. Key responsibilities include providing medical governance, managing safety events, and collaborating with internal and external stakeholders to develop groundbreaking HIV treatments.

GSK

On-site Permanent

Medical Director, ViiV Healthcare

The Medical Director role at ViiV Healthcare involves managing and reporting data from Phase 1-4 clinical trials, contributing to protocol development, and providing medical oversight and support. You will work closely with internal and external stakeholders to ensure the successful execution and interpretation of clinical studies, with a focus on advancing HIV treatments and prevention.

GSK United Kingdom

On-site Permanent

Medical Director, ViiV Healthcare

The Medical Director role at ViiV Healthcare involves managing and reporting data from Phase 1-4 clinical trials, contributing to the design and medical governance of studies, and providing medical expertise and support throughout the trial process. The role is crucial in advancing HIV treatments and working closely with internal and external stakeholders to ensure the success of clinical studies.

GSK

On-site Permanent

ViiV Healthcare (GSK) Director, Clinical Pharmacology

This role involves leading clinical pharmacology strategy across HIV drug development programs, applying PK/PD and pharmacometric modeling to inform study design, regulatory decisions, and development pathways. The Director will mentor project leads, collaborate with cross-functional teams, and serve as a scientific expert in modeling and simulation to advance ViiV’s mission-driven HIV research from early to late-stage development.

GSK United States

Hybrid Permanent

ViiV Healthcare (GSK) Director, Clinical Pharmacology

This role involves providing scientific leadership in clinical pharmacology to shape drug development programs for HIV treatments. The Director will apply PK/PD, pharmacometrics, and model-informed drug development approaches to guide study design, regulatory strategy, and key decisions across early to late-stage development. Collaboration with cross-functional teams including clinical, regulatory, biostatistics, and CMC is central to advancing innovative therapies in a mission-driven environment focused on eradicating HIV.

GSK

Hybrid Permanent

ViiV Healthcare (GSK) Director, Clinical Pharmacology

This role involves leading clinical pharmacology strategy across HIV drug development programs, applying PK/PD, pharmacometrics, and modeling to inform study design, regulatory decisions, and development pathways. The Director will mentor project leads, collaborate with cross-functional teams, and serve as a scientific expert in model-informed drug development, contributing to breakthroughs in HIV treatment and prevention.

GSK

Hybrid Permanent

Analytical Chemistry - Platform Modalities Leader

This role involves leading the strategic expansion and modernization of analytical chemistry platforms for complex therapeutic modalities, including small molecules, drug conjugates, and oligonucleotides. The Platform Modalities Leader will drive the adoption of new technologies, ensure robust and scalable analytical capabilities, and provide hands-on technical leadership while influencing cross-functional teams.

GSK Stevenage, United Kingdom

On-site Permanent

Director Medical Writing Process Management

The Director Medical Writing Process Management will lead the optimization of end-to-end business processes within Medical Writing, ensuring compliance, efficiency, and continuous improvement. They will collaborate with cross-functional teams to implement best practices, monitor process health, and align with GSK’s strategic goals.

GSK Stevenage, United Kingdom

On-site Permanent