Latest Biotech Research Scientist Jobs

Software Engineer (HPC Platform), London

As a Software Engineer focused on GPU infrastructure, you will play a key role in designing, optimizing, and managing the large-scale AI/ML infrastructure that powers Isomorphic Labs' groundbreaking research. You will collaborate with machine learning experts, biotech researchers, and various teams to ensure the reliability and efficiency of the company's AI-driven drug discovery efforts.

Isomorphic Labs London, United Kingdom

On-site Permanent

Talent Partner (Tech), London

As a Talent Partner at Isomorphic Labs, you will play a critical role in building world-class teams by developing and executing talent acquisition strategies. You will partner with senior leaders to attract top-tier talent, shape the company's future, foster an inclusive culture, and enhance the employer brand in the competitive AI and biotech landscape.

Isomorphic Labs London, United Kingdom

On-site Permanent

Director, Medical Evaluation & Case Processing Oversight

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an...

CSL

Director, Medical Evaluation & Case Processing Oversight

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an...

CSL

Labelling Strategy and Development, Oncology Team Lead

Leads a global team responsible for developing and managing oncology product labeling strategies across the R&D lifecycle. This role ensures regulatory compliance, collaborates with cross-functional stakeholders, and shapes patient-focused labeling standards while advising senior leadership and engaging with regulatory authorities to drive innovation in labeling practices.

GSK United States

Hybrid Permanent

Labelling Strategy and Development, Oncology Team Lead

Lead a global team responsible for developing and managing oncology product labelling strategies across the R&D lifecycle. This role involves shaping compliant, patient-focused labels, advising senior stakeholders, and engaging with regulatory authorities to drive innovative approaches. The position requires strong leadership, regulatory expertise, and cross-functional collaboration within a hybrid working model.

GSK

Hybrid Permanent

Head of DMPK

The Head of DMPK will lead the DMPK strategy, ensuring scientific excellence and robust human dose projections. You will collaborate with data science and ML teams to refine predictive ADME models, support external partnerships, and develop a high-performing team.

Recursion United Kingdom US$284,900 – US$400,950 pa

Hybrid Permanent

Manager, Computational Biology (Early Oncology)

Lead a team of computational biologists to integrate multi-omics data for oncology target discovery and validation, while actively contributing to analyses and mentoring team members. Drive biomarker strategy and patient stratification to advance precision oncology programs. Collaborate closely with biologists, chemists, and clinical teams to deliver data-driven insights that accelerate drug development.

Recursion United Kingdom US$151,800 – US$230,000 pa

Hybrid Permanent

Senior Counsel

The Senior Counsel provides comprehensive legal support and advice to AstraZeneca's UK marketing company, focusing on AI, data privacy, and commercial matters. They will act as a subject matter expert, draft and review legal documents, and ensure compliance with regulations and internal policies.

AstraZeneca London, United Kingdom

On-site Permanent

Senior Process Engineer

The Senior Process Engineer role at AstraZeneca involves developing and scaling up sustainable drug substance manufacturing processes. Responsibilities include introducing new equipment, optimizing processes, and collaborating with cross-functional teams to ensure robust and efficient production for clinical and preclinical trials.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent

Director Medical Writing Process Management

The Director Medical Writing Process Management will lead the optimization of end-to-end business processes within Medical Writing, ensuring compliance, efficiency, and continuous improvement. They will collaborate with cross-functional teams to implement best practices, monitor process health, and align with GSK’s strategic goals.

GSK Stevenage, United Kingdom

On-site Permanent

SERM Medical Director

The SERM Medical Director role at GSK involves providing in-depth medical and scientific expertise in safety evaluation and risk management for key GSK assets. Responsibilities include leading pharmacovigilance, developing safety strategies, and ensuring compliance with regulatory standards. The role also involves cross-functional team leadership, communication of safety issues, and contributing to the continuous improvement of safety processes.

GSK United Kingdom

On-site Permanent

SERM Scientific Director

The SERM Scientific Director will lead the safety evaluation and risk management of GSK's key assets, ensuring scientifically sound review and interpretation of data. They will develop and execute safety strategies, manage safety governance, and represent GSK on cross-functional teams to address product safety issues and improve regulatory adherence.

GSK

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

Head of Global Regulatory Affairs and Strategy

This senior leadership role involves defining and optimizing global regulatory strategies for drug development programs, building a regulatory team and systems, and implementing quality, pharmacovigilance, and medical writing frameworks. The role leverages AI to streamline regulatory workflows and ensure rapid global approval of products.

Isomorphic Labs Cambridge, United Kingdom

On-site Permanent