Discover the latest Biotechnology Jobs in the UK

Scientist/Senior Scientist, Mass Spectrometry - Generative Biology Institute

This role involves developing and optimizing LC-MS workflows for single-cell proteomics and metabolomics, supporting researchers in experimental design and data interpretation, and collaborating with multidisciplinary teams to advance cutting-edge mass spectrometry techniques. The position is ideal for a scientist who enjoys method development, troubleshooting, and translating advanced MS technologies into high-impact research.

Ellison Institute of Technology Oxford, United Kingdom £40,000 pa

On-site Permanent

Trial Vendor Senior Manager - Global Clinical Operations (GCO_

The Trial Vendor Senior Manager is a key member of the Clinical Trial Team, responsible for managing and overseeing clinical trial vendors to ensure study outcomes are met. This role involves direct operational oversight, vendor financial management, and collaboration with cross-functional teams to deliver high-quality clinical trials.

Novartis London, United Kingdom £49,140 – £91,260 pa

Associate Director, Statistical Programming

Lead a global team of statistical programmers, driving standardization, innovation, and quality in clinical trial data analysis. Develop programming strategies using modern tools like R, Git, and AI-enabled technologies, ensuring audit-ready deliverables and alignment with biostatistics and data management. Provide technical leadership and influence global drug development strategy across phases I–IV studies.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

GLP Vendor Oversight and QA Lead

This role involves overseeing the quality and compliance of external partners in GLP-regulated nonclinical research, including CROs and laboratories. Responsibilities include vendor qualification, risk-based monitoring, audit coordination, and ensuring adherence to regulatory standards. The role requires deep knowledge of GLP, GCP, and GMP regulations and strong cross-functional collaboration.

CSL

Senior Clinical Trial Case Manager

This role involves leading safety data review and pharmacovigilance activities within clinical trials, ensuring compliance with international regulations such as GxP. The individual will mentor team members, manage CAPAs, support regulatory inspections, and contribute to safety reporting and risk management. Key responsibilities include MedDRA coding, safety data analysis, and developing pharmacovigilance procedures to support global regulatory requirements.

CSL