Latest Research Scientist Jobs

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of phase 1-3 clinical trials for hematological malignancies. This role involves collaborating with a multi-disciplinary team to ensure patient safety, scientific integrity, and regulatory compliance, while contributing to the strategic development of GSK's oncology portfolio.

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

Hybrid Permanent

Senior Security Engineer, London

As a Senior Security Engineer, you will play a crucial role in architecting and managing the security of Isomorphic Labs' AI-based platform and HPC infrastructure. You will work closely with DevOps, SRE, and other teams to ensure robust security practices, from secure architecture and IaC to threat modeling and incident response.

Isomorphic Labs United Kingdom

Hybrid Permanent

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

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 and investigators.

Pfizer

On-site Permanent

Cluster HTA Hub Senior Manager

In this role, you will develop and lead complex projects, manage economic research studies for clinical trials, and formulate research plans to enhance the value of Pfizer's medicines. You will collaborate with sales teams and utilize health economic models to maximize sales and improve customer interactions.

Pfizer Poland

On-site Permanent

Clinical Development Medical Director - Neuromuscular

This role involves leading clinical development programs in neuroscience, with a focus on neuromuscular or related disorders. The Medical Director will shape clinical strategy, oversee trial execution, interpret data, and engage with regulatory and external experts to advance innovative therapies. It requires strong medical and scientific leadership within a global, cross-functional environment.

Novartis Ardross, Alba / Scotland, IV17 0YF, United Kingdom £83,510 – £155,090 pa

Hybrid Permanent

Clinical Development Medical Director - Neuromuscular

This role involves providing clinical leadership in neuroscience drug development, with a focus on neuromuscular or related neurological disorders. The Medical Director will shape global clinical strategy, lead trial execution, and guide regulatory submissions while collaborating with cross-functional teams and external experts. It emphasizes scientific innovation, particularly in gene therapy, within a dynamic, international environment.

Novartis Ireland €90,300 – €167,700 pa

Hybrid Permanent

Associate Director, Biostatistics

The role involves leading statistical strategy and execution across clinical development programs, including study design, data analysis, and regulatory submissions. The individual will provide expert statistical input, manage internal or outsourced programming teams, and represent biostatistics in interactions with global regulatory agencies. Emphasis is placed on innovation, cross-functional collaboration, and delivery of high-quality statistical outputs for clinical trials and submissions.

CSL

Hybrid Permanent

Associate Director, Biostatistics

This role leads the statistical strategy and execution for clinical development programs within a therapeutic area, ensuring robust study design, data analysis, and regulatory compliance. The Associate Director collaborates with cross-functional teams, represents biostatistics in regulatory interactions, and oversees internal or outsourced programming efforts. They also drive innovation in statistical methodologies and contribute to clinical trial interpretation and reporting.

CSL

Hybrid Permanent

Executive Director, Strategy, Oncology R&D

This role involves crafting and driving the global Oncology R&D strategy, integrating clinical, scientific, and commercial insights to shape portfolio priorities. You will advise senior leadership, optimize investment decisions, and collaborate across functions to deliver high-impact strategic outcomes.

AstraZeneca United States US$270,222 – US$405,332 pa

On-site Permanent

Executive Director, Strategy, Oncology R&D

This role involves crafting and driving the global Oncology R&D strategy, integrating clinical, scientific, and commercial insights to shape portfolio priorities. You will advise senior leadership on complex strategic topics, optimize investment decisions, and collaborate across functions to deliver impactful patient outcomes.

AstraZeneca US$270,222 – US$405,332 pa

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 collaborating with cross-functional teams to ensure compliance with US, EU, and ROW regulations.

Recursion United Kingdom £176,400 – £228,250 pa

Hybrid Permanent Flexible

Manager, Global Regulatory Science CTA

This role involves leading the operational execution of Clinical Trial Applications (CTAs) globally, outside the US, with a focus on the UK regulatory landscape. Responsibilities include managing CTA submissions, ensuring regulatory compliance, coordinating with CROs, and leveraging advanced digital tools to enhance submission efficiency.

Moderna Poland

On-site Permanent

Manager, Global Regulatory Science CTA

This role involves leading the operational execution of Clinical Trial Applications (CTAs) globally, outside the US, with a focus on the UK regulatory landscape. Responsibilities include managing CTA activities, ensuring regulatory compliance, coordinating with CROs, and leveraging advanced digital tools to enhance submission efficiency.

Moderna

On-site Permanent