Jobs in Cambridge

Senior Clinical Trial Manager, Cambridge, MA

The role involves end-to-end management of clinical trials within a fast-paced, AI-driven drug discovery environment. The Senior Clinical Trial Manager will lead cross-functional teams, oversee trial start-up through close-out, ensure compliance with ICH/GCP standards, and integrate AI innovations into clinical operations. Key responsibilities include vendor and budget management, clinical documentation, data oversight, and supporting regulatory readiness and audits.

Isomorphic Labs Cambridge, United Kingdom

Hybrid Permanent

Director of Clinical Pharmacology, Cambridge, MA

Lead clinical pharmacology strategy for small molecule programs in oncology and non-oncology areas, designing and executing studies from Phase 1 through late development. Utilize AI-driven models for PK/PD prediction, dose optimization, and regulatory submissions, while managing CROs and translating preclinical data into human dosing strategies.

Isomorphic Labs Cambridge, United Kingdom

Postdoctoral Research Associate in Nucleic Acid Computing and Molecular Engineering (Fixed Term)

The role involves designing, building, and validating programmable nucleic-acid systems for genetic privacy. The postholder will work on developing molecular systems that can measure genetic information while limiting exposure of the underlying genomic sequence, engaging in iterative experimental and computational work.

University of Cambridge Cambridge, South East England, United Kingdom £37 – £46 pa

Contract

RTSM Project Manager (Randomisation and Trial Supply Management)

The RTSM Project Manager is responsible for the design, development, testing, and maintenance of clinical studies within the RAMOS IRT system. The role involves managing complex IRT study designs, ensuring data integrity, and collaborating with internal and external stakeholders to drive continuous improvements in clinical supplies systems.

GSK

RTSM Project Manager (Randomisation and Trial Supply Management)

The RTSM Project Manager is responsible for designing, developing, testing, and maintaining clinical studies within the RAMOS IRT system. The role involves managing complex IRT study designs, ensuring data integrity, and partnering with internal and external stakeholders to drive continuous improvements in clinical supplies systems.

GSK

Senior Scientist, Automated Diagnostic Systems - Pathogen

This role involves developing and optimizing automated workflows for a sample-to-answer diagnostic platform using whole genome sequencing. The scientist will translate molecular biology processes into integrated fluidic systems, focusing on nucleic acid extraction, library preparation, and assay robustness. Collaboration with engineers and chemists is central to advancing the platform from concept to prototype.

Ellison Institute of Technology Oxford, United Kingdom

On-site Permanent

Director - Immunoassay Development

Lead the development and optimisation of quantitative immunoassays for at-home diagnostic tests, from initial design through validation and commercialisation. This hands-on leadership role involves managing scientific collaborators, ensuring regulatory compliance, and translating lab-based assays into point-of-care formats such as lateral flow and microfluidic cartridges. Work with human biological samples and drive assay performance in sensitivity, precision, and stability.

Talentmark Stevenage, Hertfordshire, United Kingdom £75,000 – £100,000 pa

Fluidic System Engineer - Pathogen

Design and develop microfluidic systems for a point-of-care diagnostic device that enables metagenomic sequencing through a cartridge-based interface. Work closely with cross-functional teams to integrate microfluidics with instrumentation, electronics, and firmware, focusing on robustness, automation compatibility, and real-world performance. Conduct prototyping, testing, and validation using techniques like soft lithography and rapid prototyping to advance decentralized infectious disease diagnostics.

Ellison Institute of Technology Oxford, United Kingdom

On-site

Senior Scientist Translational Developability

This role involves leading laboratory science to characterise and de-risk therapeutic antibody and biopharmaceutical candidates. Responsibilities include designing and running experiments, analysing data, and collaborating with multidisciplinary teams to support programme progression. The position offers hands-on lab work and opportunities for technical and leadership development.

GSK Stevenage, United Kingdom

Senior Manager - CMC RA Biopharm Development Projects

This role involves leading global CMC regulatory strategies for biopharmaceutical development projects, preparing regulatory submissions, and advising on manufacturing and quality risks. You will collaborate with cross-functional teams and interact with regulators to ensure timely submissions and supply continuity.

GSK Canterbury, United Kingdom

Senior Manager - CMC RA Biopharm Development Projects

This role involves leading global CMC regulatory strategies for biopharmaceutical development projects, preparing regulatory submissions, and advising on manufacturing and quality risks. You will work in cross-functional teams, interact with regulators, and mentor colleagues.

GSK United States

Senior Manager - CMC RA Biopharm Development Projects

This role involves leading global CMC regulatory strategies for biopharmaceutical development projects, preparing regulatory submissions, and advising on manufacturing and quality risks. You will work in cross-functional teams, represent CMC in regulatory interactions, and mentor colleagues.

GSK

Senior Manager - CMC RA Biopharm Development Projects

This role involves leading global CMC regulatory strategies for biopharmaceutical development projects, preparing regulatory submissions, and advising on manufacturing and quality risks. You will collaborate with cross-functional teams and interact with regulators to ensure timely and high-quality submissions.

GSK

Senior Manager - CMC RA Biopharm Development Projects

This role involves leading global CMC regulatory strategies for biopharmaceutical development projects, preparing regulatory submissions, and advising on manufacturing and quality risks. You will work in cross-functional teams, represent CMC in regulatory interactions, and mentor colleagues.

GSK

Senior Manager - CMC RA Biopharm Development Projects

This role involves leading global CMC regulatory strategies for biopharmaceutical development projects, preparing regulatory submissions, and advising on manufacturing and quality risks. You will work in cross-functional teams, represent CMC in regulatory interactions, and mentor colleagues.

GSK