Latest Drug Discovery Jobs

General Application - Register Your Interest

Isomorphic Labs is applying frontier AI to help unlock deeper scientific insights, faster breakthroughs, and life-changing medicines with an ambition to solve all disease.The future is coming. A future enabled and enriched by the incredible power of machine learning. A...

Isomorphic Labs United Kingdom

Support Engineer, London

As a Support Engineer, you will provide technical support, troubleshoot complex issues, and develop automation tools to improve efficiency. You will collaborate with other teams to resolve technical issues, manage 3rd party integrations, and contribute to the onboarding of new employees. This role is crucial for shaping the support strategy and driving innovation through automation.

Isomorphic Labs United Kingdom

Hybrid Permanent

Research Associate - Biology Automation

This role involves developing and running automated biochemical and cell-based assays to support drug discovery projects. You will work on a leading-edge automation platform, ensuring high-quality data and collaborating with cross-functional teams to drive small molecule therapeutics development.

Recursion Crathes, Alba / Scotland, United Kingdom

On-site Permanent

Associate Director, CMC Regulatory Affairs

This role involves leading the development and implementation of CMC regulatory strategies for small molecule drugs in global clinical trials. Responsibilities include managing CMC submissions, providing regulatory guidance, and supporting cross-functional teams in navigating international regulations.

Recursion London, W1C 2QP, United Kingdom £88,200 – £111,100 pa

Hybrid Permanent Flexible

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead clinical research activities for GSK’s oncology portfolio, focusing on advancing the development of antibody drug conjugates (ADCs) for solid tumors. Key responsibilities include collaborating with multidisciplinary teams to design and execute clinical trials, ensuring high-quality protocol development, and engaging with key external experts to drive data generation and regulatory approvals.

GSK

Hybrid Permanent

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of clinical trials for GSK's oncology portfolio, focusing on hematological malignancies. Key responsibilities include collaborating with multidisciplinary teams, ensuring patient safety, and contributing to regulatory submissions and publications.

GSK Stevenage, United Kingdom

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 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

Senior Director, Global Product Lead, Early Oncology R&D

This role involves leading global product teams in early oncology R&D, from candidate selection through Phase III investment decisions. Responsibilities include shaping development strategies, engaging stakeholders, and ensuring ethical standards in oncology research.

AstraZeneca Cambridge, United Kingdom

On-site 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

Global Regulatory Affairs Associate Director (Cardio-Metabolic)

This role involves leading the development and submission of regulatory documents, providing strategic direction, and negotiating with health authorities to expedite approvals. The position also focuses on aligning regional regulatory approaches with global objectives and managing Health Authority interactions.

Novartis

Hybrid Permanent

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

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing and executing clinical trials, creating development plans, and ensuring regulatory compliance. The role also includes collaborating with cross-functional teams, providing expert input on clinical data, and engaging with external stakeholders to drive strategic insights.

Pfizer

On-site Permanent

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

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing and executing clinical trials, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally. The role also includes providing expert input on trial design, regulatory activities, and engaging with external stakeholders to drive strategic insights.

Pfizer

On-site Permanent

(Fixed Term) Data Quality Control Specialist. Clinical Biomarker Laboratory

The Data QC Specialist will perform detailed quality control reviews of laboratory data and documentation to ensure accuracy, traceability, and compliance with regulatory standards. This role involves working closely with laboratory scientists and data management teams to resolve data discrepancies and maintain inspection readiness.

Moderna Oxford, United Kingdom

On-site Temporary

Senior Systems Engineer, GXP Systems

The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is establishing a leading research, development, and manufacturing facility at...

Moderna Oxford, United Kingdom

On-site Permanent