Latest regulatory affairs Jobs

Senior Specialist, Data Science

Job Title: Senior Specialist, Data Science — Operational Data Strategy (ODS), BioPharma R&DLocation: United KingdomCompetitive Salary & Excellent Company Benefits!Introduction to the Role:The Operational Data Strategy (ODS) function provides strategic oversight for how clinical operations data is collected, organized, validated,...

AstraZeneca Cambridge, United Kingdom

Senior Group Director, Safety Development & Processes

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive...

Roche Welwyn Hatfield, United Kingdom

Analytical Chemistry - Platform Modalities Leader

This role involves leading the strategic expansion and modernization of analytical chemistry platforms for complex therapeutic modalities, including small molecules, drug conjugates, and oligonucleotides. The Platform Modalities Leader will drive the adoption of new technologies, ensure robust and scalable analytical capabilities, and provide hands-on technical leadership while influencing cross-functional teams.

GSK Stevenage, United Kingdom

On-site Permanent

Head of Make CoE

The Head of Make CoE will lead the transformation of end-to-end manufacturing processes across a global network, partnering with sites and central teams to deliver safer, higher-quality, more sustainable, and more productive operations. Key responsibilities include strategy and roadmap leadership, governance, cross-functional integration, and team development, with a focus on digital and autonomous manufacturing.

AstraZeneca Macclesfield, United Kingdom

Hybrid 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

Executive Director, Respiratory

Leads translational biology strategy in respiratory research, integrating human-centric science to drive target validation and clinical translation across diseases like COPD, IPF, and pulmonary hypertension. Builds and leads a multidisciplinary team, leveraging internal and external capabilities to advance GSK's respiratory portfolio with a focus on mechanistic insight and biomarker integration.

GSK Stevenage, United Kingdom

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 third-party delivery and documentation, and capability building to improve speed, quality, and compliance in clinical operations.

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

Hybrid Permanent

Medical Director, Clinical Development (Oncology), Cambridge, MA

This role involves leading the clinical development of oncology drug candidates derived from AI-driven insights, translating them into actionable trial strategies, and ensuring scientific and regulatory rigor. The Medical Director will act as the primary medical monitor, guide cross-functional teams, and represent the company in interactions with regulators and key opinion leaders. The position emphasizes patient safety, protocol compliance, and strategic input from discovery through clinical proof-of-concept.

Isomorphic Labs Cambridge, United Kingdom

Hybrid 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

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

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

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

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