Biotechnology Jobs

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 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, 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

Director, Oncology Translational Medicine Project Manager

This role leads project management for GSK’s antibody-drug conjugate (ADC) translational medicine programs, integrating biomarker and diagnostic strategies across clinical development. The Director ensures cross-functional coordination, governance readiness, and operational execution across internal teams and external partners, driving strategic planning and compliance for key oncology R&D milestones.

GSK United States

Hybrid Permanent

Director, Translational Science Lead

Leads translational science strategy across renal, inflammation, fibrosis, and neurodegeneration disease areas, driving biomarker development and validation from preclinical to clinical stages. Integrates multi-omics, human tissue data, and novel technologies to inform drug development decisions and support clinical trial design. Works cross-functionally to align translational insights with research, clinical, and regulatory teams.

GSK US$178,200 – US$297,000 pa

Hybrid Permanent

Director, Translational Science Lead

This role leads translational science strategy across renal, inflammation, fibrosis, and neurodegeneration disease areas, focusing on biomarker development and validation to support clinical decision-making from preclinical through to launch. The position drives innovation in human translation using advanced technologies and multi-omics data, while providing strategic input across drug development and business development opportunities.

GSK US$178,200 – US$297,000 pa

Hybrid Permanent

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 shaping regulatory approaches and mentoring teams in a complex, science-driven environment.

GSK €90,000 – €150,000 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Lead CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Work cross-functionally to ensure compliance, support inspections, and maintain product supply. Influence regulatory decisions and mentor teams within a complex, matrixed environment.

GSK £144,375 – £240,625 pa

Hybrid Permanent

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 across cross-functional teams to ensure compliance, support inspections, and maintain product supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions in a complex, global environment.

GSK £144,375 – £240,625 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, ensuring compliance with global regulations and supporting submissions, inspections, and supply continuity. Works cross-functionally to shape regulatory approaches and mentor teams, with a focus on innovation and risk mitigation in complex regulatory environments.

GSK €90,000 – €150,000 pa

Hybrid Permanent

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

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and ensuring compliance with global regulations. Works cross-functionally to address complex CMC issues, support inspections, and influence regulatory decisions. Focuses on maintaining product supply and optimizing regulatory processes across international markets.

GSK £144,375 – £240,625 pa

Hybrid Permanent

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 across cross-functional teams to ensure compliance, support inspections, and maintain product supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions in a complex, global environment.

GSK United States US$144,375 – US$240,625 pa

Hybrid Permanent

VP, Medicine Development Leader - Respiratory

This role leads the global development of a respiratory medicine from proof of concept through to approval, serving as the primary accountable leader across a cross-functional matrix team. The VP will define strategic direction, oversee clinical and regulatory execution, and align development with GSK’s broader R&D and commercial strategy, while engaging with senior leadership and external stakeholders to advance patient-focused innovation.

GSK US$309,750 – US$516,250 pa

Hybrid Permanent

VP, Medicine Development Leader - Respiratory

Lead the global development of a respiratory medicine from clinical proof of concept through to first-market approval, serving as the single point of accountability. You will build and lead a cross-functional matrix team, define strategic direction, and ensure alignment with GSK’s R&D and commercial strategies. The role involves shaping lifecycle plans, making evidence-based go/no-go decisions, and engaging with regulators and senior leadership to deliver patient-focused medical solutions.

GSK US$309,750 – US$516,250 pa

Hybrid Permanent