Latest Innovation Jobs

Clinical Trial Supply Manager

This role involves managing the clinical trial supply chain for GSK's global R&D studies, translating protocols into operational supply strategies, and ensuring timely delivery of investigational products. The manager coordinates across depots, logistics partners, and internal teams to maintain compliance, minimise waste, and support study milestones across all phases of clinical development.

GSK €48,375 – €116,000 pa

On-site Permanent

Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for GSK's global R&D trials, translating protocols into supply strategies, and ensuring timely delivery of investigational products. The manager will lead supply planning, coordinate with depots and logistics partners, and act as the primary link between clinical teams and supply operations across Phase I–IV studies. Emphasis is placed on risk-adjusted, patient-focused planning and continuous improvement in compliance with GxP and regulatory standards.

GSK £48,375 – £116,000 pa

On-site Permanent

Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for GSK's global R&D trials, from protocol review to study close-out. The Clinical Trial Supply Manager ensures timely, compliant delivery of investigational products by translating protocols into supply strategies, managing inventory and distribution, and acting as the key link between clinical teams and supply operations across Phase I–IV studies.

GSK €48,375 – €80,625 pa

On-site Permanent

Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for global trials from protocol review to study close-out, ensuring timely delivery of investigational products while minimizing waste. The Clinical Trial Supply Manager acts as the key link between supply chain and clinical teams, developing risk-adjusted supply strategies, overseeing depot operations, and ensuring compliance with GxP and regulatory standards across Phase I–IV studies.

GSK €48,375 – €116,000 pa

On-site Permanent

Senior Clinical Project Manager

The Senior Clinical Project Manager will lead the execution of one or more clinical trials from start to finish, ensuring compliance with regulations and managing cross-functional teams. This role involves planning, budgeting, and overseeing global clinical trials, with a focus on early phase oncology studies.

Recursion United Kingdom £165,900 – £211,100 pa

Hybrid Permanent

Global Study Manager

The Global Study Manager role involves leading the operational delivery of clinical studies from initiation to archiving, ensuring timelines, quality, and budget are met. Key responsibilities include crafting delivery plans, leading the Operational Working Group, and collaborating with the Central Study Team to achieve study deliverables. The role emphasizes innovation, risk management, and stakeholder communication.

GSK United Kingdom

Hybrid Permanent

Global Study Manager

The Global Study Manager role involves leading the operational delivery of clinical studies from initiation to archiving, ensuring timelines, quality, and budget adherence. Key responsibilities include crafting delivery plans, leading the Operational Working Group, and ensuring compliance with ICH/GCP guidelines. The role emphasizes innovation, risk management, and stakeholder communication.

GSK

Hybrid Permanent

Medical Lead - Respiratory

This role involves leading the medical strategy for GSK's specialty respiratory portfolio, ensuring patient needs are at the forefront. Responsibilities include managing a medical therapy team, developing strategic plans, and engaging with healthcare professionals and regulatory bodies.

GSK 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

NIS P&D Project Management, Associate Director

The NIS P&D Project Management, Associate Director role involves developing and delivering Non-Interventional Studies (NIS) project plans, managing resources, and collaborating with various functional teams to ensure accurate and aligned project schedules. Key responsibilities include maintaining data quality in Planisware, forecasting costs, and managing risks.

GSK

Hybrid Permanent

NIS P&D Project Management, Associate Director

The NIS P&D Project Management, Associate Director is responsible for developing and delivering high-quality NIS Project Plans, managing resources, and collaborating with various functional teams to ensure alignment with R&D and marketed product portfolios. The role involves maintaining accurate project schedules, forecasting costs, and ensuring data quality in Planisware.

GSK

Hybrid Permanent

NIS P&D Project Management, Associate Director

The NIS P&D Project Management, Associate Director is responsible for developing and delivering high-quality Non-Interventional Studies (NIS) project plans, managing resources, and collaborating with various functional teams. Key responsibilities include maintaining accurate project schedules, driving cost and resource forecasts, and ensuring alignment with strategic goals.

GSK

Hybrid Permanent

Regional Regulatory Intelligence Manager

This role involves leading the regional regulatory intelligence strategy, ensuring alignment with global regulatory direction and Health Authority expectations. Responsibilities include identifying and translating regulatory intelligence into actionable insights, influencing regulatory outcomes, and driving cross-functional collaboration to embed intelligence into submission processes and templates.

GSK United Kingdom

Hybrid Permanent

Regional Regulatory Intelligence Manager

This role involves leading the regional regulatory intelligence strategy, ensuring alignment with global regulatory direction and Health Authority expectations. Responsibilities include identifying and translating regulatory intelligence into actionable insights, influencing regulatory outcomes, and driving cross-functional collaboration to embed intelligence into submission processes and templates.

GSK

Hybrid Permanent

Regional Regulatory Intelligence Manager

This role involves leading the regional regulatory intelligence strategy, ensuring alignment with global regulatory direction and Health Authority expectations. Responsibilities include identifying and translating regulatory intelligence into actionable insights, driving cross-functional collaboration, and supporting capability building and training.

GSK

Hybrid Permanent