Latest Drug Discovery Jobs

Vice President, Head of Clinical Operations

This role involves leading the clinical operations strategy and execution across Recursion’s development portfolio, from study planning to study closeout. You will build and mentor a high-performing team, manage global trials, and ensure operational excellence in an AI-native TechBio company.

Recursion United Kingdom

On-site Permanent

Vice President, Medical Affairs

As Vice President, Medical Affairs, you will lead the development and execution of integrated medical strategies for Recursion's clinical portfolio, focusing on areas like oncology, rare diseases, and immunology. You will collaborate with cross-functional teams to build evidence, engage key stakeholders, and ensure the translation of scientific insights into meaningful patient impact.

Recursion North Tyneside, NE29 8EP, 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

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 regulatory leads, partnering on global strategies, and representing the function in senior interactions and health authority meetings.

AstraZeneca Canterbury, United Kingdom

On-site 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 mentoring regulatory professionals, partnering with directors on global strategies, and representing the Global Regulatory Affairs function in senior interactions and health authority meetings.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Global Labelling Director, Content (Immunology)

The Global Labelling Director, Content (Immunology) will lead the development and delivery of high-quality global labelling strategies for innovative medicines. Key responsibilities include developing core labelling documents, collaborating with cross-functional teams, and ensuring compliance with regulatory requirements. The role involves representing global labelling in governance forums and contributing to decision-making discussions.

Novartis

Hybrid Permanent

Global Program Safety Team Lead

This role involves leading the Medical Safety organization for Novartis' Neuroscience division, managing safety strategies, and influencing high-stakes decisions. Responsibilities include managing disease areas, enhancing team expertise, and ensuring robust safety evaluations throughout the product lifecycle.

Novartis United Kingdom

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

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with internal and external teams to ensure studies are on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and supplies.

GSK Stevenage, United Kingdom

Hybrid Permanent

CMC Leader (Director)

Leads end-to-end CMC strategy and execution for a pharmaceutical product from early development through commercialisation, including process development, regulatory filings, and lifecycle planning. Coordinates cross-functional global teams across R&D, supply chain, and regulatory to deliver clinical and commercial supply, ensuring technical transfer, quality compliance, and launch readiness. Focuses on complex modalities such as small molecules and oligonucleotides, with strong emphasis on regulatory strategy, risk management, and transition to commercial operations.

GSK Stevenage, United Kingdom

Hybrid Permanent

CMC Leader (Director)

Leads the development, industrialization, and lifecycle delivery of a physical medicine from early development through commercialization, ensuring seamless transition across stages. Coordinates cross-functional CMC and supply chain teams to deliver regulatory filings, process validation, and launch readiness, with a focus on complex products including small molecules and oligonucleotides. Drives strategic decision-making across R&D, manufacturing, and commercial functions to ensure timely, compliant, and scalable product supply.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

Small Molecule CMC Leader - Senior Director

Leads Chemistry, Manufacturing and Controls (CMC) strategy and execution for small molecule, biopharm, or cell and gene therapy medicines from late-stage development through commercialisation. Oversees process development, regulatory filings, supply chain, and lifecycle management across global teams and external partners, ensuring readiness for approval and launch. Role involves high-level governance engagement, risk management, and transition to commercial supply.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working closely with internal and external teams to ensure studies are delivered on time, on budget, and in compliance with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK Poland

Hybrid Permanent