Latest Research Scientist Jobs

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead clinical research activities to advance GSK’s oncology portfolio. Key responsibilities include developing and executing phase 1-3 clinical trials, collaborating with cross-functional teams, and engaging with key external experts to ensure the successful development and regulatory approval of innovative oncology treatments.

GSK United States

Hybrid Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the clinical research activities for GSK’s oncology portfolio, including developing and executing phase 1-3 clinical trials. They will collaborate with various stakeholders to ensure high-quality protocol development, medical monitoring, and data interpretation, while also engaging with key external experts and thought leaders.

GSK

Hybrid Permanent

Senior Alliance Manager, London

This role involves managing and nurturing strategic scientific and business partnerships in a cutting-edge AI-driven drug discovery environment. The Senior Alliance Manager will oversee alliance governance, align internal and external teams, and ensure successful delivery of collaborative research and development programs. The position plays a key role in scaling operational frameworks and fostering a collaborative culture across high-impact partnerships.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Bioinformatics Engineer, London

This role involves building and maintaining a high-fidelity biological data layer to support machine learning at Isomorphic Labs. You will develop large-scale bioinformatics pipelines, harmonize public and internal datasets, and collaborate with cross-functional teams to ensure data quality and standardization. Your work will directly accelerate drug discovery by providing robust, integrated biological data for AI-driven research.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to the study team. The position also involves mentoring others and contributing to strategic discussions with key stakeholders.

Pfizer

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and collaboration with internal and external stakeholders.

Pfizer

On-site 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

Global Medical Affairs Director, Autoimmune Diseases

The Global Medical Affairs Director is responsible for developing and implementing strategic and operational programs for autoimmune diseases, focusing on innovative evidence, launch readiness, and post-market solutions. They lead medical-scientific input, evidence generation, and stakeholder engagement to maximize the value of new medicines and support global medical affairs initiatives.

Novartis

Hybrid Permanent

(Fixed Term) Warehouse Specialist

In this hands-on role, you will ensure seamless warehouse and logistics support within a 24/7 GMP environment at Moderna’s UK manufacturing facility. You will manage inventory, coordinate deliveries, and maintain compliance with safety and operational standards, directly supporting mRNA vaccine production.

Moderna Oxford, United Kingdom

On-site Permanent Shift-work

(Fixed Term) Warehouse Specialist

This role involves operating in a 24/7 GMP environment at Moderna’s UK manufacturing facility, ensuring seamless warehouse and logistics support. Responsibilities include managing inventory, verifying deliveries, coordinating shipments, and maintaining compliance with safety and operational standards.

Moderna

On-site Contract Shift-work

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

Associate Director, Biostatistics (2)

The Associate Director, Biostatistics, leads the statistical contribution to clinical development programs, ensuring appropriate methodologies for study design, data analysis, and regulatory submissions. They collaborate with cross-functional teams, manage outsourcing operations, and represent Biostatistics in regulatory interactions.

CSL United Kingdom

On-site Permanent

Associate Director, Biostatistics (2)

The Associate Director, Biostatistics, leads the statistical contribution to clinical development programs, defining statistical strategies, ensuring appropriate methodologies, and collaborating with cross-functional teams. They also manage outsourcing operations, represent Biostatistics in regulatory interactions, and support innovation in clinical trial design and analysis.

CSL

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, leading resource planning, and representing the function in senior interactions and health authority meetings.

AstraZeneca United States

On-site Permanent

Associate Director, Regulatory Affairs

This role involves leading the development of global regulatory strategies for drug development programs, managing regulatory activities, and collaborating with cross-functional teams. The position requires extensive experience in regulatory affairs, with a focus on global health authorities and regulatory submissions.

Recursion North Tyneside, NE29 8EP, United Kingdom

On-site Permanent