Latest Medical Services 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

Vice President, Build — Data, Engineering & AI

Role purposeThe VP, Build — Data, Engineering & AI is the owner of the International Commercial build engine, accountable for turning prioritized demand into trusted, reusable and production-grade data, AI agents, solutions and technical services. The role owns the International...

Pfizer

Vice President, Build — Data, Engineering & AI

Role purposeThe VP, Build — Data, Engineering & AI is the owner of the International Commercial build engine, accountable for turning prioritized demand into trusted, reusable and production-grade data, AI agents, solutions and technical services. The role owns the International...

Pfizer London, EC1R 0EH, United Kingdom

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Works cross-functionally to ensure compliance, support inspections, and maintain product supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions across complex international environments.

GSK £144,375 – £240,625 pa

Hybrid Permanent

Small Molecule CMC Leader - Senior Director

Lead CMC strategy and execution for small molecule drug development from Phase 2 through commercialization, managing cross-functional teams and global regulatory filings. Oversee tech transfer, process scale-up, and lifecycle planning while ensuring compliance with US, EU, and international standards. Interface with senior leaders and health authorities to drive successful product launches and post-approval activities.

GSK

Hybrid Permanent

Director DDS Business Enablement & Implementation

This role involves leading high-impact transformation initiatives within Drug Development and Supply (DDS) at GSK, focusing on process optimization, organizational change, and performance enablement. The Director will act as a cross-functional integrator, driving strategic programs and ensuring adoption of new ways of working across a complex, matrixed biopharma environment.

GSK US$173,250 – US$288,750 pa

Hybrid Permanent

MSAT Molecule Steward

This role involves providing end-to-end technical leadership for a pharmaceutical product throughout its lifecycle, from development through manufacturing and commercial supply. The Molecule Steward ensures product quality, process robustness, and regulatory compliance by leading technical strategy, coordinating cross-functional teams, and driving continuous improvement across global supply chain sites. The position requires deep scientific expertise, strong leadership in matrixed environments, and active involvement in regulatory submissions and lifecycle management.

GSK €103,500 – €172,500 pa

Hybrid Permanent

MSAT Molecule Steward

This role involves end-to-end technical leadership for a pharmaceutical product across its lifecycle, from development through manufacturing and commercialization. The Molecule Steward ensures product quality, robustness, and compliance by leading technical strategy, process optimization, and cross-functional collaboration across R&D, manufacturing, and regulatory teams. They play a key role in technology transfer, continuous process verification, and maintaining control strategies in a highly regulated environment.

GSK €103,500 – €172,500 pa

Hybrid Permanent

MSAT Molecule Steward

This role involves providing end-to-end technical leadership for a pharmaceutical product across its lifecycle, from development through manufacturing and commercialization. The Molecule Steward ensures product quality, regulatory compliance, and process robustness by leading cross-functional teams, defining control strategies, and driving continuous improvement initiatives. It requires deep scientific expertise, strong leadership in matrixed environments, and coordination across R&D, manufacturing, and regulatory functions.

GSK €103,500 – €172,500 pa

Hybrid Permanent

MSAT Molecule Steward

This role involves providing end-to-end technical leadership for a pharmaceutical product throughout its lifecycle, from development to commercial manufacturing. The Molecule Steward ensures product quality, robustness, and manufacturability by leading technical strategy, process optimization, and regulatory compliance across global supply chain teams. The position requires deep scientific expertise, cross-functional collaboration, and leadership in resolving complex technical challenges in a regulated environment.

GSK €103,500 – €172,500 pa

Hybrid Permanent

Privacy Lead – R&D / Chief Patient Office (CPO)

This role involves leading privacy strategy and compliance for R&D and patient-focused initiatives at GSK, ensuring responsible data use in clinical research, digital health, and AI-driven projects. The Privacy Lead embeds privacy-by-design principles, conducts risk assessments, and supports governance across highly regulated environments, balancing innovation with ethical data practices.

GSK

Hybrid Permanent

Senior Manager - CMC Regulatory Affairs Biopharm Development Projects

This role involves leading CMC regulatory activities for GSK's investigational, late development, and early commercial products. Responsibilities include driving CMC strategy, preparing regulatory documents, managing project activities, mentoring staff, and engaging with external agencies to ensure compliance and expedite submissions.

GSK Canterbury, United Kingdom

On-site Permanent

Senior Director Clinical Operations Asset Lead - Hepatology, renal and cardiovascular disease

This role leads clinical operations for high-impact, complex global trials in hepatology, renal, and cardiovascular disease, with a focus on late-phase outcomes studies and rare diseases. The position shapes operational strategy, drives innovation in trial design, and ensures delivery across a diverse asset portfolio. It involves leading vendor partnerships, managing regulatory and quality compliance, and developing clinical teams within a patient-ambitious, data-driven environment.

GSK Stevenage, United Kingdom US$242,550 – US$404,250 pa

Hybrid Permanent

Senior Manager - CMC Regulatory Affairs Biopharm Development Projects

This role involves leading CMC regulatory activities for GSK's investigational, late development, and early commercial products. Responsibilities include driving CMC strategy, preparing regulatory documents, managing project activities, and mentoring staff. The position requires a strong understanding of regulatory requirements and the ability to communicate complex issues across departments and with external agencies.

GSK

On-site Permanent