Biotechnology Jobs

Executive Medical Director, Clinical Development Lead - Oncology

This role leads the clinical strategy for oncology assets across their lifecycle, defining the scientific narrative, benefit-risk framework, and decision-making approach. The Executive Medical Director acts as a strategic partner within cross-functional teams, drives governance decisions, and represents Clinical Development in internal and external forums. They integrate clinical, regulatory, and commercial considerations while leveraging AI and advanced analytics to accelerate data-driven development in cancer therapies.

GSK US$242,250 – US$403,750 pa

Hybrid Permanent

Executive Medical Director, Clinical Development Lead - Oncology

This role leads clinical strategy and scientific vision for an oncology asset across its lifecycle, serving as the primary clinical authority within GSK's Medicine Development Team. The Executive Medical Director shapes integrated clinical development plans, drives data-informed decision-making using advanced analytics, and represents Clinical Development in governance, regulatory, and external partnership settings. They are responsible for aligning scientific, regulatory, and commercial strategies while mentoring clinical talent and advancing innovation in development models.

GSK US$242,250 – US$403,750 pa

Hybrid Permanent

Executive Medical Director, Clinical Development Lead - Oncology

This role leads clinical strategy for an oncology asset within GSK’s R&D pipeline, defining the scientific narrative, benefit-risk framework, and development roadmap across the lifecycle. The Executive Medical Director serves as the primary clinical authority, shaping strategic decisions, engaging with health authorities, and leveraging advanced analytics to accelerate impactful cancer treatments. They will also mentor talent and drive innovation in clinical development models.

GSK

Hybrid Permanent

Executive Medical Director, Clinical Development Lead - Oncology

This role leads clinical strategy for oncology assets across their lifecycle, defining the scientific narrative and benefit-risk framework while serving as the primary clinical authority. The position shapes enterprise-level decision-making, integrates real-world evidence and AI-driven insights, and represents Clinical Development in governance and regulatory discussions. It emphasizes strategic leadership over operational delivery, with a focus on innovation and talent development in a matrix environment.

GSK US$242,250 – US$403,750 pa

Hybrid Permanent

Manager, Labelling Strategy and Development

This role involves leading the development and maintenance of global product labelling, including prescribing information and patient leaflets, for pharmaceutical products. The manager will collaborate with cross-functional teams to ensure accurate, compliant, and scientifically sound labelling across international markets, supporting medicines throughout their lifecycle. Key responsibilities include authoring regulatory documents, aligning labelling strategy, and mentoring team members within a global regulatory environment.

GSK United Kingdom

Hybrid Permanent

VP and Head of Operational Effectiveness

This role leads operational effectiveness across GSK’s R&D organisation, focusing on accelerating clinical trial delivery through data-driven performance frameworks, process reimagination, and transformational programs. The position drives continuous improvement in ways of working, builds organisational capability, and ensures compliance and operational excellence across key functions such as third-party management, clinical documentation, and project management. It plays a strategic role in benchmarking performance, realising value from transformation initiatives, and embedding a culture of innovation and accountability at scale.

GSK United Kingdom €190,500 – €317,500 pa

Hybrid Permanent

Quality Assurance & Regulatory Affairs Specialist - MedTech

This role involves ensuring quality assurance and regulatory compliance for advanced medical devices throughout their design and manufacturing lifecycle. The specialist will conduct internal audits, support regulatory submissions across Europe, North America, and APAC, and help shape QA processes in line with ISO 13485 and CE marking standards. The position is central to bringing innovative, life-saving medical technologies to market in a fast-paced, autonomous environment.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom £45,000 – £49,000 pa

On-site Permanent

VP and Head of Operational Effectiveness

Leads operational effectiveness for clinical trial delivery across GSK’s R&D organisation, driving process reimagination, performance intelligence, and transformation programs to accelerate development timelines. Focuses on data-driven insights, operational excellence in key capabilities like third-party management and documentation, and culture change to enable best-in-class performance. Works across global teams to embed continuous improvement and technology adoption at scale.

GSK €190,500 – €317,500 pa

Hybrid Permanent

VP and Head of Operational Effectiveness

This role leads operational effectiveness for GSK’s R&D organization, focusing on accelerating clinical trial delivery through data-driven performance frameworks, process redesign, and transformation programs. The VP will drive measurable improvements in speed, quality, and compliance across development operations, while building capabilities in areas like third-party management, eTMF, and project management. The position requires integrating advanced analytics, leading large-scale change, and fostering a culture of continuous improvement to support GSK’s global R&D ambitions.

GSK €190,500 – €317,500 pa

Hybrid Permanent

VP and Head of Operational Effectiveness

Lead the design and execution of operational effectiveness strategies across GSK’s R&D organisation, focusing on clinical trial delivery, process transformation, and performance analytics. Drive measurable improvements in speed, quality, and compliance by reimagining ways of working, building capabilities, and leveraging data-driven insights. Oversee key operational functions including third-party management, clinical documentation, and project management support to ensure high-quality, efficient outcomes aligned with global priorities.

GSK €190,500 – €317,500 pa

Hybrid Permanent

VP and Head of Operational Effectiveness

Leads operational effectiveness for clinical trial programs across GSK’s R&D organisation, driving process reimagination, performance intelligence, and transformation to accelerate drug development. Focuses on data-driven insights, operational excellence in key capabilities like third-party management and eTMF, and cultural change to improve speed, compliance, and quality. Works globally with senior leadership to deliver measurable improvements aligned with strategic goals.

GSK

Hybrid Permanent

VP and Head of Operational Effectiveness

Leads operational effectiveness for clinical trial programs across GSK’s R&D organisation, driving process transformation, performance intelligence, and capability building to accelerate drug development. Focuses on data-driven insights, operational excellence in areas like third-party management and eTMF, and large-scale change initiatives to improve speed and quality. Works at a global senior leadership level to embed a culture of continuous improvement and innovation.

GSK €190,500 – €317,500 pa

Hybrid Permanent

CMC Leader (Director)

Leads end-to-end CMC and supply chain strategy for a physical medicine from pre-clinical development through commercialisation, including process development, regulatory filings, and lifecycle planning. Works across global matrix teams to deliver robust manufacturing processes, ensure PAI readiness, and transition responsibilities to commercial operations. Focuses on complex products such as small molecules or oligonucleotides, integrating technical, regulatory, and supply considerations.

GSK

Hybrid 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

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