Latest Recruitment Jobs

Senior Director Clinical Operations Asset Lead - Hepatology, renal and cardiovascular disease

This role leads clinical operations for complex, multi-indication assets in hepatology, renal, and cardiovascular disease, with strategic oversight of global Phase III trials, rare disease programmes, and co-development partnerships. The position involves shaping operational strategy, managing high-level vendor relationships, and driving innovation in trial design including decentralised and hybrid models. It requires leadership in risk management, data-driven decision-making, and team development within a global regulatory and compliance framework.

GSK United Kingdom US$242,550 – US$404,250 pa

On-site Permanent

Senior Director Clinical Operations Asset Lead - Hepatology, renal and cardiovascular disease

This role leads clinical operations for high-complexity assets in hepatology, renal, and cardiovascular disease, with a focus on global Phase III outcomes trials, rare disease programmes, and co-development partnerships. The position drives end-to-end operational strategy, including country and site selection, patient recruitment, risk management, and vendor oversight, while ensuring alignment with clinical development and evidence generation plans. It also involves direct leadership of clinical teams, fostering innovation in trial design, and maintaining inspection readiness across the portfolio.

GSK US$242,550 – US$404,250 pa

On-site Permanent

Senior Scientist or Associate Principal Scientist Metabolist Team

This role involves conducting advanced in vitro and ex vivo research to identify and validate therapeutic targets for obesity. The successful candidate will work in a dynamic, collaborative environment, designing and implementing experiments, analyzing data, and contributing to drug discovery projects across multiple sites.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Regulatory Affairs Assistant

The Regulatory Affairs Assistant will provide administrative, operational, and compliance support to the Regulatory Affairs team, ensuring accurate data and documentation, supporting team processes, and maintaining compliance with regulatory standards. The role involves a broad range of activities, including regulatory file compilation, database management, project coordination, and administrative support to the Head of Regulatory and the team.

AstraZeneca London, United Kingdom

On-site Permanent

Director, Clinical Pharmacology

This role involves leading the clinical pharmacology and pharmacometrics strategy for rare disease and oncology programs. Responsibilities include designing clinical studies, authoring regulatory documents, and collaborating with cross-functional teams to expedite drug development.

Recursion North Tyneside, NE29 8EP, United Kingdom US$212,900 – US$297,000 pa

Hybrid Permanent

Vice President, Head of Strategy & Operations

Your work will change lives. Including your own.The Impact You'll MakeRecursion is reimagining drug discovery through the integration of automated cell biology, high-dimensional data, and AI-driven analytics. As Head of Strategy & Operations, you will be our CEO's closest strategic...

Recursion North Tyneside, NE29 8EP, United Kingdom

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

Head of RII or Oncology Programming

This role involves leading the clinical data programming for GSK's Respiratory, Immunology & Inflammation or Oncology Research Unit. Responsibilities include setting high standards for data quality, driving innovation with technologies like Generative AI, and collaborating with cross-functional teams to accelerate the development and submission of new medicines and vaccines.

GSK United Kingdom

On-site Permanent

Head of RII or Oncology Programming

This role involves leading the clinical data programming for GSK's Respiratory, Immunology & Inflammation or Oncology Research Unit. Responsibilities include setting high standards for data quality, driving innovation with technologies like Generative AI, and collaborating with cross-functional teams to accelerate the development and submission of medicines and vaccines.

GSK

On-site Permanent

Head of RII or Oncology Programming

This senior leadership role involves overseeing the transformation of clinical data into regulatory-ready evidence for GSK's Respiratory, Immunology & Inflammation, or Oncology Research Units. The Head of Programming will lead a global team, drive strategic initiatives, and champion innovation in clinical programming, ensuring high standards of quality and compliance.

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