Jobs in London

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

Project Specialist (External Manufacturing-Drug Product)

This role involves managing technology transfer projects for external drug product manufacturing, coordinating between GSK and Contract Manufacturing Organisations (CMOs) to ensure timely and compliant delivery. The specialist will drive project schedules, mitigate risks, align cross-functional teams, and maintain governance across the supply chain, particularly for sterile drug products like monoclonal antibodies and vaccines. A key focus is ensuring technical knowledge retention and operational readiness for new suppliers or assets.

GSK United Kingdom €69,600 – €116,000 pa

Hybrid Permanent

Project Specialist (External Manufacturing-Drug Product)

The role involves managing technology transfer projects for external manufacturing of drug products, coordinating between GSK and Contract Manufacturing Organisations (CMOs). The specialist ensures timely delivery of critical path activities, aligns internal and external stakeholders, and maintains governance across procurement, quality, technical, and supply functions, particularly for sterile drug products like monoclonal antibodies and vaccines.

GSK €69,600 – €116,000 pa

Hybrid Permanent

Medical Director, Clinical Development (Oncology), Cambridge, MA

This role involves leading the clinical development of oncology drug candidates derived from AI-driven insights, translating them into actionable trial strategies, and ensuring scientific and regulatory rigor. The Medical Director will act as the primary medical monitor, guide cross-functional teams, and represent the company in interactions with regulators and key opinion leaders. The position emphasizes patient safety, protocol compliance, and strategic input from discovery through clinical proof-of-concept.

Isomorphic Labs Cambridge, United Kingdom

Hybrid Permanent

Research Associate, Compound Management

The Research Associate will manage inventory, prepare reagents, and run automated systems for high-throughput screening. They will collaborate with cross-functional teams to optimize workflows and adopt new technologies, contributing to the company's drug discovery platform.

Recursion United Kingdom

On-site Permanent

Compound Management Inventory Specialist (Contractor)

This role involves managing compound inventory and supporting high-throughput screening by preparing precise compound plates through automated systems. The specialist will maintain organization across multiple storage locations and ensure accurate, efficient fulfillment of experimental requests in a fast-paced, tech-driven drug discovery environment.

Recursion United Kingdom

On-site Contract

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

Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism)

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

Novartis London, United Kingdom

Hybrid Permanent

Senior Principal Developer

This role involves developing and maintaining R packages and Shiny applications to support clinical trial data analysis and reporting. The developer will collaborate with statisticians and clinical teams to build automated, reproducible tools, while promoting open-source practices and responsible AI integration. Emphasis is placed on modernizing workflows through user-centric design, documentation, and deployment in production environments.

Novartis £57,050 – £105,950 pa

Remote Permanent

Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism)

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

Novartis

Hybrid Permanent

Global Program Clinical Head (Neuroscience)

As a Global Program Clinical Head, you will lead the development and execution of clinical programs in Neuroscience, collaborating with global teams to ensure regulatory compliance and patient-centric outcomes. You will define clinical strategies, manage cross-functional teams, and engage with external stakeholders to advance transformative therapies.

Novartis Spain

Hybrid Permanent

Global Program Clinical Head (Neuroscience)

As a Global Program Clinical Head, you will lead end-to-end clinical development programs in Neuroscience, driving strategy, execution, and regulatory compliance. You will collaborate with global teams, define innovative development plans, and ensure high-quality, patient-centric clinical trials.

Novartis Ireland

Hybrid Permanent