Latest Drug Discovery Jobs

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

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Recursion United Kingdom

Director, Clinical Pharmacology

This role involves leading the clinical pharmacology and pharmacometrics strategy for rare disease and oncology programs, designing clinical studies, and interfacing with cross-functional teams and health authorities. The position requires a Ph.D., M.D., or Pharm D. with 5-9+ years of experience in drug development, proficiency in modeling software, and strong collaboration skills.

Recursion London, United Kingdom £118,300 – £136,500 pa

Hybrid Permanent

SERM Scientific Director, Oncology

The SERM Scientific Director role involves leading pharmacovigilance and risk management strategies for clinical development and post-marketing products. Responsibilities include evaluating safety data, managing safety concerns, and supporting regulatory activities. The role operates in a global, cross-functional environment and may include mentoring responsibilities.

GSK United Kingdom

Hybrid Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead clinical research activities for GSK’s oncology antibody drug conjugate (ADC) portfolio, focusing on advancing the development of clinical trials from early to late stages. Key responsibilities include protocol development, medical monitoring, safety data review, and collaboration with a multi-disciplinary team of experts to ensure the scientific integrity and timely delivery of clinical trials.

GSK

Hybrid Permanent

Director, Process Engineering & Packaging

Leads process engineering and packaging for biologics at AstraZeneca, driving development of clinical and commercial drug product processes including fill/finish, device assembly, and packaging. Manages a team of scientists and engineers, oversees technology transfer across internal and external manufacturing sites, and advances design for manufacturability and regulatory strategies. Focuses on innovation, scale-up, and technical excellence within a global biopharmaceutical manufacturing network.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Senior Global Clinical Operations Director

This role leads the operational strategy and end-to-end delivery of global clinical programs in oncology, spanning early and late-phase development. The director will drive trial design, cross-functional collaboration, and regulatory readiness while managing complex multinational studies, CRO partnerships, and high-performing teams. Emphasis is placed on innovation, efficiency, and patient impact through advanced trial methodologies and strategic leadership.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

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

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing, executing, and interpreting clinical studies, creating development plans, and collaborating with cross-functional teams to ensure regulatory approvals and global market access. The role also includes specialized monitoring, regulatory submissions, and engaging with external stakeholders to drive strategic insights.

Pfizer

On-site Permanent

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

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine, working closely with cross-functional teams to design, execute, and interpret clinical studies. Key responsibilities include creating clinical development plans, regulatory submissions, and providing expert input on trial design and execution, while ensuring compliance and strategic insight generation.

Pfizer

On-site Permanent

(Fixed Term) Laboratory Technician, Clinical Biomarker Laboratory, Immunoassay

The Laboratory Technician will support the Immunoassays group by executing experimental work, maintaining the lab, and ensuring high-quality data for clinical trials. The role involves hands-on lab work, assay development, and collaboration with multiple projects, with a focus on safety and regulatory compliance.

Moderna Oxford, United Kingdom

On-site Contract

Associate Director, CMC Regulatory Science, International

This role involves developing and implementing CMC regulatory strategies for global submissions, providing guidance on regulatory CMC aspects, and ensuring compliance with health authority guidelines. The candidate will support multiple programs in various therapeutic areas, including vaccines, oncology, and rare diseases, and work closely with manufacturing and quality teams.

Moderna London, United Kingdom

On-site Permanent

Senior Scientific Writer II

The Senior Scientific Writer II role involves developing high-quality medical and scientific communications for Novartis, including slide decks, congress materials, and advisory board content. The position requires strong collaboration with cross-functional teams to ensure content accuracy, consistency, and compliance with internal and external standards.

Novartis London, United Kingdom

Hybrid Permanent

Global Medical Affairs Director, Autoimmune Diseases

The Global Medical Affairs Director leads strategic and operational programs for autoimmune diseases, focusing on innovative evidence, launch readiness, and post-market solutions. They develop and execute medical/scientific engagement strategies, provide expert input on clinical trials, and collaborate with internal and external stakeholders to maximize the value of Novartis medicines.

Novartis London, United Kingdom

Hybrid Permanent