Latest GSK Jobs

Director, Oncology Clinical Biomarkers

This role involves developing and implementing biomarker strategies for late-stage oncology clinical trials, collaborating with cross-functional teams to identify patient populations and optimize drug development. The Director will leverage cutting-edge technologies and methodologies to validate biomarkers and inform clinical decisions.

GSK Stevenage, United Kingdom £189,750 – £316,250 pa

On-site Permanent

SME - MSAT EM Technical Operations DS/DP

This role involves collaborating with internal and external stakeholders to support the commercial manufacture of large molecule drug substances and sterile drug products. Responsibilities include executing technical strategies, managing product lifecycle activities, and ensuring compliance with GMP standards. The role also involves supporting CMOs in audits, technical transfers, and continuous improvement initiatives.

GSK East Hertfordshire, United Kingdom

On-site Permanent

Programming Leader

The Programming Leader role involves overseeing project-level and study-level programming strategy and delivery for multiple complex studies in GSK's global pipeline. You will collaborate with cross-functional teams, ensure high-quality outputs, and champion the adoption of agile principles and new technologies to improve efficiency and data analysis.

GSK Stevenage, United Kingdom

Hybrid Permanent

Manager, Translational Biomarker Data Pathways & Re-use

This role involves leading the setup, stabilization, and scaling of end-to-end translational data pathways, ensuring biomarker datasets are reusable and accessible. Key responsibilities include resolving systemic barriers, aligning data delivery with decision timelines, and developing repeatable processes for data re-use across multiple functions.

GSK Stevenage, United Kingdom

Hybrid Permanent

Director, DP Workstream Leader – Small Molecule Parenteral (LAIs and Oligos)

Leads drug product development for sterile long-acting injectables and oligonucleotides, guiding cross-functional teams in formulation, process development, and technology transfer. Ensures robust CMC strategies, regulatory compliance, and supply readiness across clinical to commercial phases. Focuses on delivering high-quality, patient-centric medicines through scientific leadership and matrix collaboration.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

Director, DP Workstream Leader – Small Molecule Parenteral (LAIs and Oligos)

Leads late-stage drug product development for sterile long-acting injectables and oligonucleotides, guiding cross-functional teams in formulation, process development, and technology transfer. Translates CMC and regulatory strategies into actionable plans, ensuring robust control strategies and compliance across clinical and commercial phases. Works within a matrix environment to align R&D, manufacturing, and supply chain functions for successful asset delivery.

GSK Stevenage, United Kingdom

Hybrid Permanent

VP, Medicine Development Leader - Respiratory

This role leads the global development of a respiratory medicine from clinical proof of concept through to approval, serving as the strategic and operational leader of a cross-functional matrix team. The VP Medicine Development Leader defines the asset’s vision, drives evidence-based decision-making, and ensures alignment across R&D, manufacturing, regulatory, and commercial functions to deliver differentiated medicines for patients. The position involves shaping development plans, managing budgets, engaging with regulators, and supporting lifecycle strategies while representing the asset to senior leadership and external stakeholders.

GSK Stevenage, United Kingdom US$309,750 – US$516,250 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating submissions and ensuring compliance with global regulations. Works across cross-functional teams to address complex regulatory challenges and support continuous supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions in a matrix environment.

GSK Stevenage, United Kingdom €90,000 – €150,000 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for pharmaceutical 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 projects.

GSK London, United Kingdom £90,000 – £150,000 pa

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working closely with internal and external teams to ensure studies are delivered on time, on budget, and in compliance with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK Poland

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Key responsibilities include monitoring study conduct, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Responsibilities include monitoring study progress, drafting key documents, coordinating meetings, managing communications, and overseeing clinical supplies and budget tracking.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are delivered on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, managing study communications, and overseeing clinical supply and investigational product delivery.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Responsibilities include monitoring study progress, drafting key clinical documents, coordinating meetings, managing study communications, and overseeing clinical supply and investigational product delivery.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are delivered on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK

Hybrid Permanent