Jobs in Cambridge

VP, Medicine Development Leader - Specialty Product Development

Leads the global development of a medicine from clinical proof of concept to approval, serving as the single point of accountability. Builds and leads a cross-functional matrix team to define strategy, drive evidence generation, and support regulatory and lifecycle planning. Interfaces with senior leadership and external stakeholders to advance patient-focused medical solutions.

GSK £242,250 – £403,750 pa

Associate Director of Clinical Sciences

Lead clinical sciences strategy and execution for global oncology studies, with responsibility for end-to-end protocol development, clinical data review, and cross-functional collaboration. Focus on immuno-oncology with strong emphasis on regulatory compliance, patient safety, and scientific leadership across clinical development phases. Work within a matrix environment to guide study design, interpretation, and regulatory submissions.

GSK Stevenage, United Kingdom

Senior Director, Future CMC Dossier Strategy

This role leads the strategic transformation of CMC regulatory submissions at GSK, shaping the future of dossier development through innovation in automation, Generative AI, and structured data. The Senior Director will drive alignment across regulatory, quality, manufacturing, and technology functions, championing initiatives like ICH M4Q and Project Sonata. It involves influencing senior governance, leading change, and building next-generation regulatory processes in a global, science-driven environment.

GSK United Kingdom £193,500 – £322,500 pa

Senior Director, Future CMC Dossier Strategy

Leads the strategic transformation of CMC regulatory submissions at GSK, driving innovation through automation, Generative AI, and structured data. Works cross-functionally to align regulatory strategy with development and enterprise initiatives, including ICH M4Q and Project Sonata. Focuses on modernising the 'CMC dossier of tomorrow' within a global matrix environment.

GSK

Sr Director/Director and Team Lead, Global Regulatory Strategy - LCM

Leads the development and execution of global regulatory lifecycle strategies for assigned assets, ensuring alignment with GSK's medicine development plans and regulatory requirements across key markets. Acts as the primary regulatory point of contact on cross-functional teams, drives innovation in regulatory approaches, and provides strategic input to business development and crisis management. Directly manages a team and collaborates with senior leaders and health authorities worldwide.

GSK United Kingdom

Hybrid Permanent

Senior Medical Director, Oncology Clinical Development - GU

Leads clinical development for oncology assets, focusing on genitourinary (GU) cancers, with responsibility for designing and executing global Phase 1-3 trials. Works cross-functionally to generate clinical evidence, engage key external experts, and support regulatory submissions and product launches. Operates in a matrix environment across strategy, medical affairs, and regulatory teams.

GSK Switzerland PLN 593,250 – PLN 988,750 pa

Hybrid Permanent

Senior Medical Director, Oncology Clinical Development - GU

This role involves leading clinical development for oncology therapeutics, specifically in genitourinary (GU) cancers, within a global matrix environment. The Senior Medical Director will design and execute Phase 1-3 clinical trials, ensure scientific integrity of study data, and engage with internal and external experts to advance GSK’s oncology portfolio. The position requires deep expertise in medical oncology, strong leadership in cross-functional teams, and active involvement in regulatory and strategic initiatives.

GSK PLN 593,250 – PLN 988,750 pa

Hybrid Permanent

Senior Director, Future CMC Dossier Strategy

This role leads the strategic transformation of CMC regulatory submissions at GSK, shaping the future of dossier development through innovation in automation, Generative AI, and structured data. The Senior Director will drive alignment across regulatory, development, quality, and technology functions, acting as a key liaison for enterprise-wide initiatives like Project Sonata and ICH M4Q. The position is central to modernising regulatory processes and establishing next-generation submission standards globally.

GSK £141,750 – £236,250 pa

Senior Director, Translational Genetics

Leads a team of translational genetics scientists to integrate genetic, genomic, and clinical data in support of drug discovery and development. Focuses on addressing key translational questions using statistical genetics and innovative analytical approaches across therapeutic areas such as respiratory, immunology, and neurodegeneration. Works within cross-functional teams and establishes external collaborations to advance GSK's R&D pipeline.

GSK

Hybrid Permanent

Associate Director, Device Lead

Lead the technical ownership and global delivery of medical device platforms within GSK's manufacturing network, ensuring compliance with regulatory standards and driving innovation in device technology. Collaborate across R&D, supply chain, and quality functions to manage device lifecycle, technology transfer, and risk. Work with suppliers and internal teams to optimize manufacturing processes and support combination product development.

GSK United States £142,725 – £237,875 pa

Associate Director, Device Lead

Lead the technical ownership and lifecycle management of medical device platforms within GSK's global supply chain, ensuring regulatory compliance, technology transfer from R&D, and robust supply strategies. Drive innovation in drug delivery devices and combination products while collaborating across global teams on quality, manufacturing efficiency, and risk management. Serve as the primary technical interface between device suppliers and internal MSAT teams.

GSK £142,725 – £237,875 pa

Senior Director, Future CMC Dossier Strategy

This role leads the strategic transformation of CMC regulatory submissions at GSK, shaping the future of dossier content and processes through initiatives like ICH M4Q and Project Sonata. The individual will drive innovation using automation, structured data, and Generative AI while aligning regulatory, development, and quality functions. It involves high-level stakeholder engagement and governance input across a global matrix organization.

GSK

Hybrid Permanent

Senior Director, Translational Genetics

Leads a team of translational genetics scientists to drive data-driven insights supporting drug discovery and development across key therapeutic areas. Applies advanced statistical genetics and integrates genomics and clinical data to address translational questions. Fosters innovation, external collaborations, and scientific leadership within a multidisciplinary environment.

GSK US$207,075 – US$345,125 pa

Hybrid Permanent

Senior Director, Translational Genetics

Leads a team of translational genetics scientists to integrate genetic, genomic (especially proteomics), and clinical data in support of drug discovery and development. Focuses on addressing key translational questions across therapeutic areas such as respiratory, hepatology, neurodegeneration, and immunology. Works within cross-functional teams and drives external scientific collaborations to advance GSK’s R&D pipeline.

GSK US$207,075 – US$345,125 pa

Hybrid Permanent

Senior Director, Future CMC Dossier Strategy

This role leads the strategic transformation of CMC regulatory submissions at GSK, focusing on next-generation approaches including ICH M4Q implementation, automation, and Generative AI. The individual will drive alignment across regulatory, quality, manufacturing, and technology functions to shape the future of regulatory dossiers. It involves high-level stakeholder engagement, change leadership, and innovation in a global, matrixed environment.

GSK £538,500 – £897,500 pa