Latest Managed Services Jobs

Steriles Standards Manager

Leads the development and enforcement of operational standards for sterile manufacturing, ensuring compliance with regulatory requirements and driving continuous improvement. Works cross-functionally with quality, engineering, and operations teams to standardize processes, support audit readiness, and strengthen control in aseptic environments. Focuses on reducing variability, improving compliance, and coaching teams in a highly regulated pharmaceutical setting.

GSK Barnard Castle, United Kingdom

On-site Permanent

Site Shift Manager

This role involves leading 24/7 manufacturing operations outside core hours at GSK’s Barnard Castle site, ensuring safety, compliance, and supply chain continuity. The Site Shift Manager acts as the primary on-site leader during shifts, coordinating production, managing incidents, and aligning cross-functional teams including manufacturing, quality, and engineering. Emphasis is placed on real-time decision-making, audit readiness, and continuous improvement in a regulated pharmaceutical environment.

GSK Barnard Castle, United Kingdom

On-site Permanent

Vice President, Strategy, Value & Innovation

Role purposeThe VP, Strategy, Value & Innovation drives what International Commercial’s Digital & AI capacity works on, why it matters, and how value is realized. The role owns the portfolio system, investment logic framework, go/no-go gates, benefits ledger, external innovation...

Pfizer

Vice President, Strategy, Value & Innovation

Role purposeThe VP, Strategy, Value & Innovation drives what International Commercial’s Digital & AI capacity works on, why it matters, and how value is realized. The role owns the portfolio system, investment logic framework, go/no-go gates, benefits ledger, external innovation...

Pfizer London, EC1R 0EH, United Kingdom

Head of RII or Oncology Programming

This senior leadership role involves overseeing the transformation of clinical data into regulatory-ready evidence for GSK's Respiratory, Immunology & Inflammation, or Oncology Research Units. The Head of Programming will lead a global team, drive strategic initiatives, and champion innovation in clinical programming, ensuring high standards of quality and compliance.

GSK

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

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

ViiV Healthcare (GSK) Senior Director, Clinical Development

As the Senior Medical Director, 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 advance ViiV Healthcare's mission of eradicating HIV, focusing on long-acting medicines and novel approaches to treatment and prevention.

GSK

On-site Permanent

Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for global R&D trials, translating protocols into operational supply strategies, and ensuring on-time delivery of investigational products. The Clinical Trial Supply Manager acts as the key link between clinical teams and supply operations, overseeing demand planning, depot management, and compliance across Phase I–IV studies, including investigator-sponsored and compassionate use trials.

GSK Stevenage, United Kingdom €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 studies, translating protocols into operational supply strategies, and ensuring timely delivery of investigational products. The manager will coordinate across depots, logistics partners, and clinical teams to maintain supply continuity, minimise waste, and support study milestones across phases I–IV. It requires strong planning, risk management, and GxP compliance in a patient-focused, global trial environment.

GSK Belgium €69,600 – €116,000 pa

On-site Permanent

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