Latest Oncology Jobs

Medical Director, Oncology Clinical Development

This role involves leading oncology clinical trials from protocol design to study reporting, ensuring scientific integrity and alignment with regulatory and commercial goals. The Medical Director will collaborate with global experts and internal teams to advance GSK’s oncology pipeline, with a focus on data generation, safety monitoring, and strategic medical input across the clinical development lifecycle.

GSK Stevenage, United Kingdom US$222,750 – US$371,250 pa

Hybrid Permanent

Medical Director, Oncology Clinical Development

Leads clinical development of oncology assets through trial design, execution, and data interpretation, ensuring scientific integrity and regulatory compliance. Engages with external experts and cross-functional teams to advance GSK’s oncology pipeline. Focuses on generating robust clinical evidence to support approvals and lifecycle management.

GSK United States

Hybrid Permanent

Manager, Oncology Regulatory Strategy

Lead regional regulatory strategy for oncology products across the Rest of World (ROW) region, aligning with global teams to ensure timely submissions, approvals, and commercially favorable labeling. Partner with project teams and health authorities to shape regulatory positions and influence the regional environment. Ensure compliance and effective implementation of regulatory standards throughout the product lifecycle.

Pfizer United Kingdom

Associate Director, Computational Biology – Early Discovery

Lead a team of computational biologists to identify and validate novel oncology targets using integrated phenomics, transcriptomics, genomics, and proteomics data. Develop and scale methods for target discovery in oncology and immunological diseases, collaborating closely with biologists, data scientists, and engineers. Drive data strategy and present findings to stakeholders to advance drug discovery programs.

Recursion United Kingdom

On-site Permanent

Director, Clinical Pharmacology

Lead clinical pharmacology and pharmacometrics strategy across rare disease and oncology programs, designing studies and supporting regulatory submissions. Oversee modeling and simulation to inform dose selection and development decisions, working closely with cross-functional teams in a TechBio environment powered by AI-driven drug discovery. Serve as the primary expert in regulatory interactions related to clinical pharmacology.

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

Hybrid Permanent

Senior Scientist (In vivo Pharmacology & Translational Sciences), Cambridge, MA

Lead translational strategies for oncology and immunology programs by designing in vivo pharmacology and PK/PD studies to validate AI-designed drug candidates. Bridge computational predictions with experimental validation through CRO partnerships and biomarker-driven approaches. Drive preclinical data generation to inform clinical trial design and regulatory filings.

Isomorphic Labs England

Hybrid Permanent

Associate Director, CMC Regulatory Science, International

Lead the development and execution of CMC regulatory strategies for mRNA-based products across global submissions, including IND/CTA/BLA/MAA filings. Provide expert guidance on regulatory compliance, interact with health authorities, and support quality and manufacturing teams through change controls and submissions. Work within a multidisciplinary team at the Harwell site to advance Moderna’s pipeline in vaccines, oncology, and rare diseases.

Moderna London, United Kingdom

On-site Permanent

Principal Scientist, Immunogenicity and Ligand Binding Assays

This role involves leading and executing phase-appropriate bioanalytical strategies for immunogenicity and ligand binding assays (LBA) within Moderna’s mRNA-LNP therapeutic pipeline. The Principal Scientist will oversee assay development, validation, and sample analysis, ensuring regulatory compliance and scientific rigor across clinical programs. The position emphasizes collaboration with cross-functional teams, integration of emerging technologies including AI-enabled tools, and contribution to regulatory submissions and data interpretation in a GcLP-compliant environment.

Moderna Oxford, United Kingdom

Hybrid Permanent

Senior Director, Targets and Mechanisms Solutions

Leads the strategic direction and AI-driven innovation of Pfizer’s Targets and Mechanisms platforms, overseeing global teams to deliver scalable, data-centric solutions that accelerate drug discovery. Integrates advanced technologies like AI, predictive analytics, and omics data to support target identification and translational research across therapeutic areas. Focuses on building interoperable digital ecosystems and embedding AI into core R&D workflows.

Pfizer Cambridge, United Kingdom US$230,900 – US$384,800 pa

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