Latest Innovation Jobs

Principal Medical Writer

This role involves authoring and delivering high-quality clinical regulatory documents, leading cross-functional teams, and managing complex writing projects. The Principal Medical Writer will interpret clinical and statistical data, ensure compliance with regulatory requirements, and contribute to global regulatory submissions.

GSK Stevenage, United Kingdom

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, CMC Regulatory Affairs

Lead the development and execution of CMC regulatory strategy for small molecule drugs in global clinical trials and marketing applications. Author and manage high-quality regulatory submissions across the US, EU, and rest of world, while advising cross-functional teams on compliance, risk mitigation, and regulatory best practices. Support clinical trial materials and GMP inspections, ensuring alignment with evolving global regulations.

Recursion North Tyneside, NE29 8EP, United Kingdom £207,500 – £280,720 pa

Remote Permanent

Director, Regulatory Affairs

This role involves leading global regulatory strategy for drug development programs, managing regulatory submissions across all stages of development, and ensuring compliance with international health authorities. The Director will collaborate with cross-functional teams to identify regulatory risks, guide clinical development, and shape the future of regulatory science using innovative technology-driven approaches in a fast-paced TechBio environment.

Recursion North Tyneside, NE29 8EP, United Kingdom £207,500 – £280,720 pa

Remote Permanent

Director, CMC Regulatory Affairs

Lead the development and execution of global CMC regulatory strategies for small molecule drugs in clinical trials and marketing applications. Author and manage high-quality regulatory submissions across the US, EU, and rest of world, while advising cross-functional teams on compliance, risk mitigation, and evolving GMP standards. Collaborate closely with internal and external stakeholders to ensure timely delivery of regulatory deliverables and support clinical development programs.

Recursion London, W1C 2QP, United Kingdom

Remote Permanent

Programme Manager (Engineering - Capital Projects)

The Capital Projects’ Programme Manager sits within the Barnard Castle site’s Engineering Projects team. The position provides experienced, visible programme management for the delivery of complex capital programmes and projects within a highly-regulated manufacturing environment. The role liaises with and...

GSK Barnard Castle, United Kingdom

EHS Platform Lead - Cority SaaS (12-Month Secondment

This role involves leading the governance and optimisation of GSK’s global Cority SaaS platform, with a focus on the Occupational Health module. The individual will drive simplification, define a global roadmap, and align EHS, technology, and compliance stakeholders to improve system scalability, user experience, and business value. Key activities include managing system enhancements, ensuring regulatory compliance, and enabling adoption through improved processes and training.

GSK United Kingdom

Hybrid Contract

Sr. Manager, Site Budgets and Contracts

The RoleReporting to the Director, Global Clinical Operations (GCO) Business Analytics & Operations Management (BAOM), the Senior (Sr.) Manager, Site Budgets & Contracts will focus on the generation and review of investigator site budgets related to investigator grants (IGs) using...

Moderna Oxford, United Kingdom

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of clinical trials for hematological malignancies, collaborating with a multidisciplinary team to ensure patient safety, scientific integrity, and regulatory compliance. This role involves medical monitoring, data review, and strategic partnerships with thought leaders in the oncology field.

GSK United States

Hybrid Permanent

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of phase 1-3 clinical trials for hematological malignancies. This role involves collaborating with a multi-disciplinary team to ensure patient safety, scientific integrity, and regulatory compliance, while contributing to the end-to-end development of oncology drugs.

GSK

Hybrid Permanent

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of phase 1-3 clinical trials for hematological malignancies. This role involves collaborating with a multi-disciplinary team to ensure patient safety, scientific integrity, and regulatory compliance, while contributing to the strategic development of GSK's oncology portfolio.

GSK

Hybrid Permanent

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of clinical trials for GSK's oncology portfolio, focusing on hematological malignancies. Key responsibilities include collaborating with multidisciplinary teams, ensuring patient safety, and contributing to regulatory submissions and publications.

GSK

Hybrid Permanent

Head of Health Economics and Outcomes

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

Associate Director, Diagnostic Planning Lead - Oncology

This role leads diagnostic planning initiatives within GSK’s Oncology Translational Medicine team, coordinating cross-functional efforts across clinical development, regulatory, and external partners to advance diagnostic assets. The position ensures alignment of project timelines, manages risks, and supports regulatory submissions, leveraging expertise in biomarkers and in vitro diagnostics within an oncology context.

GSK United States US$151,500 – US$252,500 pa

Hybrid Permanent

Associate Director, Diagnostic Planning Lead - Oncology

This role leads diagnostic planning initiatives within GSK’s Oncology Translational Medicine team, coordinating cross-functional projects and external partnerships to advance biomarker and diagnostic development. The position ensures alignment across clinical, regulatory, and commercial stakeholders, manages timelines and budgets, and supports regulatory submissions. It requires expertise in diagnostics, project management, and oncology drug development.

GSK US$151,500 – US$252,500 pa

Hybrid Permanent