Jobs in London

Team Leader, Medicinal Drug Design, London

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 London, United Kingdom

Team / Research Leader, Computational Drug Design, London

This role involves leading the design of novel small molecule therapeutics using cutting-edge AI and computational chemistry. The Team / Research Leader will define scientific direction, manage drug discovery programs, integrate AI/ML into workflows, and mentor a high-performing team.

Isomorphic Labs United Kingdom

Hybrid Permanent

Global Labelling Director, Content

The Global Labelling Director, Content will lead the development and delivery of high-quality global labelling strategies for innovative medicines. Key responsibilities include shaping labelling content, maintaining core documents, and collaborating with cross-functional teams to ensure regulatory compliance and successful product submissions.

Novartis London, United Kingdom

Hybrid Permanent

Portfolio Innovation Director - Global Clinical Operations

Leads innovation in global clinical operations by identifying and integrating AI-driven and technology-enabled solutions into clinical trials. Focuses on improving trial design, patient access, and operational efficiency while working across cross-functional teams to scale impactful innovations. Requires deep clinical and drug development expertise to evaluate and implement transformative solutions.

Novartis Ireland

Hybrid Permanent

ViiV Healthcare (GSK) Senior Director, Clinical Development

As a Senior Medical Director at ViiV Healthcare, you will lead the design and delivery of early development plans for HIV treatments, ensuring clinical excellence and medical governance across Phase 1-4 studies. You will collaborate with internal and external stakeholders to design, execute, and interpret clinical studies, focusing on long-acting medicines and ensuring patient safety and data integrity.

GSK United States

On-site Permanent

ViiV Healthcare (GSK) Senior Director, Clinical Development

This role involves leading the design and delivery of early development plans for HIV treatments, ensuring clinical excellence and medical governance across Phase 1-4 studies. You will collaborate with internal and external stakeholders to design, execute, and interpret clinical studies, ensuring patient safety and scientific excellence.

GSK

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

Senior Clinical Trial Manager

Manages clinical trial operations from start-up to closure, coordinating with CROs and internal teams to ensure timely delivery of trials in oncology and rare diseases. Focuses on process improvements and operational excellence within a fast-paced, AI-driven drug discovery environment.

Recursion London, United Kingdom £62,400 – £84,000 pa

Hybrid Permanent

Global Program Regulatory Manager - Neuroscience

This role involves driving regulatory strategy and execution for neuroscience products across global markets, with a focus on preparing and submitting clinical trial applications, managing health authority interactions, and ensuring compliance throughout the product lifecycle. The manager will work cross-functionally to translate scientific data into regulatory submissions and support timely approvals. It is a hybrid role based in London, requiring strong expertise in pharmaceutical regulatory affairs.

Novartis

Hybrid Permanent

Global Labelling Manager, Content (Neuroscience)

The Global Labelling Manager, Content will lead the development and maintenance of high-quality global labelling documents for pharmaceutical products. Key responsibilities include organising cross-functional discussions, conducting research on competitor labels, and ensuring compliance with regulatory standards across different markets.

Novartis

Hybrid Permanent

Global Labelling Associate Director, Content (Oncology)

This role involves developing and maintaining global labelling strategies and core documents for oncology products. You will lead cross-functional discussions, present proposals to governance bodies, and ensure compliance with regulatory requirements across global markets.

Novartis

Hybrid Permanent

Global Labelling Director, Content (Immunology)

The Global Labelling Director, Content (Immunology) will lead the development and delivery of high-quality global labelling strategies for innovative medicines. Key responsibilities include developing core labelling documents, collaborating with cross-functional teams, and ensuring compliance with regulatory requirements. The role involves representing global labelling in governance forums and contributing to decision-making discussions.

Novartis

Hybrid Permanent

Global Labelling Associate Director, Content (Established Products)

This role involves developing and maintaining global labelling strategies and core documents for pharmaceutical products. You will lead cross-functional discussions, present labelling proposals, and ensure compliance with regulatory requirements across different markets.

Novartis

Hybrid Permanent

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing compliance oversight for clinical programs and trials, ensuring adherence to Good Clinical Practice standards. You will act as a primary compliance partner to Clinical Trial Teams, enabling decision-making on complex regulatory scenarios and leading cross-functional discussions to resolve quality issues.

Novartis Ireland

Hybrid Permanent

Senior Principal Developer

This role involves developing and maintaining R packages and Shiny applications to support clinical trial data analysis, automation, and reporting workflows. The developer will collaborate with statisticians and clinical teams to deliver efficient, reproducible tools, while promoting best practices in data science and software development. A strong focus is placed on responsible AI integration, open-source collaboration, and modernizing clinical reporting through user-centric design and tooling.

Novartis London, United Kingdom £57,050 – £105,950 pa

Hybrid Permanent