Latest Life Sciences Jobs

Global Medical Affairs Director Hepatology

This role involves leading global medical strategy in hepatology, shaping evidence generation and scientific communication plans, and collaborating across R&D, regulatory, and market access teams. The position drives patient-focused medical initiatives, ensures robust scientific training, and optimizes external engagement with healthcare professionals, payors, and regulators. It offers leadership growth within a therapy area poised for innovation.

GSK United Kingdom €126,750 – €211,250 pa

Hybrid Permanent

Global Medical Affairs Director Hepatology

Lead the development and execution of global medical strategy in hepatology, aligning with local market needs and driving evidence generation and scientific communication. Collaborate across R&D, regulatory, and market access teams to optimize clinical care and deliver impactful medical plans. Build relationships with key stakeholders including healthcare professionals, patients, and regulators to advance patient-centred outcomes.

GSK €126,750 – €211,250 pa

Hybrid Permanent

Director, Data Product Centre of Excellence

This role leads the strategic development and governance of AI-ready data products within a global, regulated environment. The Director will establish enterprise standards, drive adoption across federated teams, and build a scalable operating model for data product delivery. The position emphasizes automation, compliance, interoperability, and measurable value realization across the data lifecycle.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Process Engineer - Drug Substance Manufacture (DSM)

This role involves optimizing chemical manufacturing processes for drug substances in a regulated pharmaceutical environment. The engineer will lead process improvements, scale-up projects, and technology transfers while ensuring compliance with safety, quality, and environmental standards. Work includes root-cause analysis, change control management, and cross-functional collaboration to enhance capacity, robustness, and efficiency in API production.

AstraZeneca Macclesfield, United Kingdom

Hybrid Permanent

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

This role involves planning, designing, and executing real-world evidence studies to support the commercial success and market positioning of GSK's oncology products. The Director will collaborate with internal and external stakeholders to ensure the generation of high-quality, scientifically credible evidence that meets regulatory and payer requirements.

GSK

On-site Permanent

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

This role involves planning and executing real-world evidence studies to support the commercial success of GSK's oncology products. The Director will work closely with medical and commercial teams to ensure that evidence is aligned with regulatory and payer requirements, and will be responsible for managing timelines, budgets, and deliverables.

GSK

On-site Permanent

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

This role involves planning and executing real-world evidence studies to support the launch and market positioning of GSK's oncology products. The Director will work closely with medical and commercial teams to ensure the generation of high-quality evidence that meets regulatory and payer requirements, driving successful patient access and commercial outcomes.

GSK

On-site Permanent

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

This role involves planning and executing real-world evidence studies to support the launch and commercial success of GSK's oncology products. The Director will collaborate with internal and external stakeholders to ensure the generation of high-quality, scientifically credible evidence that meets regulatory and market requirements.

GSK

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

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

AI Strategy Director, Development Operations

The AI Strategy Director role involves driving the AI-native Development Operations strategy at GSK, focusing on identifying and deploying AI solutions to improve clinical trial outcomes. Responsibilities include prioritizing AI opportunities, evaluating vendor capabilities, and leading cross-functional teams to prototype and deploy AI-enabled workflows.

GSK United Kingdom

On-site Permanent

AI Strategy Director, Development Operations

The AI Strategy Director role involves driving the AI-native Development Operations strategy at GSK, focusing on identifying and deploying AI solutions to accelerate clinical trials and improve patient outcomes. Key responsibilities include prioritizing AI opportunities, evaluating external vendors, and shaping deployment strategies with cross-functional teams.

GSK

On-site Permanent