Biotechnology Jobs

• Oxford
• On-site
• £40,000 pa
• Entry level

Develops generative protein design models that capture enzyme dynamics and function, designing conformationally dynamic catalysts. Runs computational and statistical analyses, publishes findings, and collaborates with in vivo evolution teams across the institute. Also mentors PhD students and research assistants and pursues translational and IP opportunities.

• London
• On-site
• £47,500 pa
• Entry level
• Contract

Investigates how protein machines remodel microtubules using cryo-electron microscopy, protein reconstitution and fluorescence microscopy. As an early member of a new lab, you will shape the research programme, establish experimental approaches and develop scientific independence while working closely with the group leader.

Cryo-EM

• London
• Hybrid · 3 days in office
• Lead

Owns safety assessment strategy for drug discovery projects from inception to regulatory submission, working with small molecule and biologics platforms. Designs screening cascades, authors IND packages, and manages CRO relationships for outsourced wet-lab work. Also guides development of an AI predictive toxicology platform with ML researchers.

AI/ML · AlphaFold

• London
• £47,500 pa
• Entry level
• Contract

Lead a computational project studying how driver mutation clones interact with their microenvironment in chronic liver disease and liver cancer. Develop graph neural networks, transformers and generative AI methods on large-scale spatial genomics, single-cell and imaging data, embedded across the Crick and Wellcome Sanger Institute with joint supervision.

PyTorch · JAX · NumPy +2

• Oxford
• On-site
• Permanent

Supports the design, construction and commissioning of new plant science laboratories, greenhouses and growth facilities. Coordinates project plans, equipment scoping and procurement, supplier quotations, deliveries and installation, and maintains readiness checklists and stakeholder communications across research and technical teams.

• Cambridge, United States
• Hybrid · 3 days in office
• Senior · manages people

Experienced medicinal chemists lead portfolio drug discovery projects from initiation to clinical candidate selection, working as Project Lead or Medicinal Chemistry Lead. They partner closely with ML scientists to refine the AI drug design platform, manage CRO resources, and may line-manage teams of 2-4 chemists.

AlphaFold

• Leeds
• Hybrid
• Senior
• Permanent

On-site CRA role monitoring Phase I–Ib studies inside a 100-bed Leeds Clinical Research Unit, covering pre-study, initiation, routine monitoring and close-out visits. Works alongside clinic, pharmacy and lab teams during first-in-human dosing days, using integrated eSource and EDC systems to focus on data integrity and protocol compliance rather than mechanical SDV.

eSource · EDC

• London
• Hybrid
• Lead · manages people

Serves as the clinical trial pharmacy subject matter expert across global oncology programmes, advising on investigational product handling, preparation, storage and accountability, and on hazardous drug and CSTD requirements. Develops pharmacy manuals and training for site pharmacists and study teams, supports audits and CAPAs, and oversees FSP pharmacists and external vendors. Hybrid role spanning London, Paris or Cambridge MA.

Closed System Transfer Devices

• Manchester
• Mid-level

Conducts site qualification, initiation, monitoring and close-out visits for clinical trials, ensuring GCP compliance, patient safety and data integrity. Builds relationships with investigators, resolves data queries, mentors junior staff and travels up to 40-60% within the region. Embedded in a sponsor-dedicated functional service partnership model.

Investigator Site Files · Trial Master Files

• Bath
• Mid-level

Conducts site qualification, initiation, monitoring and close-out visits for a CRO embedded within pharmaceutical sponsor teams, ensuring GCP compliance, patient safety and data integrity. Manages site relationships, recruitment strategies, TMF/ISF documentation and risk escalation, with mentoring of junior staff and up to 40-60% regional travel.

Investigator Site Files · Trial Master Files

• Uxbridge
• Hybrid
• Senior

An individual contributor role conducting non-interventional real-world data research for medical and HEOR teams across international markets. You will identify data sources, oversee statistical programming in R, and interpret and present findings to stakeholders. The position requires deep expertise in observational data analysis and offers hybrid working from Uxbridge.

R · GitHub · Claude +2

• London
• On-site
• Permanent

Runs a high-throughput sample processing pipeline, performing DNA extraction, normalisation and library preparation on soil, faecal and other environmental samples. Operates automated liquid handling platforms such as Myra9, logs everything in Benchling LIMS, and carries out QC checks while supporting R&D protocol testing in a CL2 lab.

Benchling · Myra9 · Hamilton +2

• Newcastle upon Tyne
• £48,337 – £68,817 pa
• Senior
• Contract

Lead an independent research programme in transplant immunology, focusing on kidney transplantation injury and new therapies, while collaborating with nine senior investigators and the NIHR Blood and Transplant Research Unit. Contribute 0.2 WTE to undergraduate and postgraduate teaching and PhD supervision within the Translational and Clinical Research Institute.

Transplant Biobank

• Stevenage
• Hybrid
• £26,000 – £40,000 pa
• Mid-level
• Permanent

Field-based role installing, maintaining and servicing nano-flow cytometry instruments at customer sites across the UK and Europe, plus remote phone and email troubleshooting of hardware, software and reagents. Involves preventative maintenance scheduling, service documentation, spare parts inventory and coordinating service contracts with the sales team, following training with senior technical staff.

Nano-flow Cytometry · nFCM

• United Kingdom
• Remote
• Senior
• Permanent

Provides clinical quality oversight and a single point of Quality contact for client study teams, partnering with Clinical Operations and Pharmacovigilance to identify, assess and mitigate risks to participant safety and reporting compliance. Co-chairs Joint Quality Councils, analyses QA metrics and audit/inspection trends, and drives quality risk management across a portfolio. Fully remote role with up to 25% travel.