Biotechnology Jobs

• Stevenage
• Hybrid · 2 days in office
• US$242,250 – US$403,750 pa
• Director

Accountable for end-to-end clinical development of a multi-tumor oncology asset, from first-in-human through registrational trials, regulatory approval and initial market launch. Acts as senior clinical representative at governance forums and leads cross-functional, matrixed teams spanning research, precision medicine, medical affairs and commercial. Requires deep antibody-drug conjugate and global health authority experience.

AI/ML

• Waltham, United States
• Hybrid · 2 days in office
• US$242,250 – US$403,750 pa
• Director · manages people

Accountable for end-to-end clinical development strategy for a multi-tumor oncology asset, spanning first-in-human through registrational trials, regulatory approval and initial launch. Acts as senior clinical representative at governance forums and leads cross-functional collaboration across research, precision medicine, medical affairs and commercial in a global matrix.

AI/ML

• London
• Hybrid · 3 days in office
• Senior

Lead the hardening and scaling of an inference platform serving fleets of cutting-edge ML models for scientific applications. Set strategy and roadmaps, architect next-generation services to solve scaling limits, and partner with research, product and operations teams to align infrastructure with biotech R&D cycles.

Kubernetes · Google Cloud Platform · NVIDIA GPU +1

• Leeds
• Hybrid
• Entry level
• Internship

A student placement supporting the Clinical Operations team in day-to-day coordination of clinical studies, including maintaining the Trial Master File (TMF/eTMF), tracking activities in CTMS, generating reports and distributing study supplies. Based in Leeds with flexibility to work remotely, though onsite working is preferred and may be required.

TMF · eTMF · CTMS +4

• Oxford
• On-site
• Mid-level
• Contract

Designs and delivers immunogenicity and bioanalytical strategies for regulated clinical programmes, developing ADA, nAb, PK and PD assays using ELISA, MSD and cell culture. Works with multidisciplinary teams to validate assays, manage reagents and SOPs, and integrate digital and AI-enabled tools. Site-based at Harwell within a growing mRNA-focused team.

ELISA · MSD · LIMS +2

• Norwich
• £21,805 pa
• Entry level
• Contract

A PhD studentship using historical DNA and whole-genome sequencing to study how red squirrel populations in Britain declined, were rescued by translocations, and lost native ancestry. The student will sequence modern and museum specimens, analyse genetic diversity, inbreeding and genetic load over time, and receive training in molecular biology, bioinformatics and population genetics.

• Oxford
• On-site
• Senior

Sole-contributor scientist role developing and executing biochemical and molecular biology assays for PK/PD analysis, spanning genomic DNA/RNA isolation, qPCR, ddPCR, RNA sequencing, MSD, ELISA and immunoblotting. Works within Moderna's Clinical Bioanalytical team at Harwell, Oxfordshire, ensuring GcLP-compliant assay qualification and validation, troubleshooting with external CRO partners, and building internal and external mRNA-based bioanalytical capability.

MSD · LIMS · eLNB +1

• Cambridge
• £80,000 – £100,000 pa
• Senior

Job Title: Senior QA Validation EngineerLocation - Cambridge: On Site (some flex on occasionSalary - £80k - £100k (depending on experience) + up to 10% bonus (company performance dependent) + equityOverviewWe are seeking an experienced Senior QA Validation Engineer to…

• Uxbridge
• Hybrid
• Senior · manages people

Technical lead on assigned clinical studies, shaping SDTM strategies from protocol review through to global regulatory submission. Involves root cause analysis, cross-functional collaboration, data integration from CRF and non-CRF sources, and engagement with SDTM automation, metadata-driven processes and agentic AI workflows. Also provides quality oversight to team members and manages CRO and vendor programming activities.

Pinnacle 21

• London
• On-site
• Junior

Hands-on lab role in a biology team, running experiments across process development, product testing and platform R&D, maintaining iPSC lines and differentiation cultures, and sharing lab operations duties. Data generated feeds directly into how processes and platforms evolve, with structured training from SOP-based work towards independent execution.

Excel · GraphPad Prism

• London
• On-site
• Mid-level

Owns end-to-end purchasing, invoicing and inventory for both electromechanical automation systems and GMP-grade sterile fluidic consumables, spanning supplier qualification, cost-down programmes and demand planning. Reports to the Hardware Lead and works across manufacturing, biology, engineering, quality and finance, building ERP/MRP-based planning in a hands-on, on-site role.

ERP · MRP

• Cambridge
• Hybrid
• Senior

Hands-on bioanalytical role developing, optimising and running LC-MS/MS assays for small and large molecule DMPK studies in an early discovery setting, analysing matrices such as plasma, blood, brain, bile, faeces and urine. Combines complex mass spectrometry troubleshooting and method development with leading scientific projects, mentoring colleagues and driving novel assay innovation in a matrix team.

UPLC-MS · LC-MS/MS · Mass Spectrometry

• London
• Hybrid
• Director

Lead global regulatory strategy for renal therapy programs across all development phases, serving as the regulatory representative on cross-functional teams. Drive major submissions such as INDs, NDAs, BLAs and MAAs, and lead health authority interactions, while mentoring regulatory team members. Distinct for its international scope and focus on renal, nephrology and rare disease assets.

IND · CTA · NDA +2

• Leeds
• Hybrid
• Senior
• Permanent

Leads data management activities across early phase trials, including healthy volunteer and patient populations, multi-site studies and reduced timelines. Accountable for all DM deliverables, resource allocation, client relationships and scope changes, while mentoring the internal study team and adopting new DM technologies.

• Maidenhead
• Hybrid
• Senior · manages people
• Permanent

Technical lead for all data management activities on late phase (IIb-III) clinical trials, from start-up through completion. Develops Data Management and Quality Management Plans, designs CRF/eCRF and database structures, and coordinates edit checks and discrepancy management. Acts as client liaison, tracking cycle times and metrics while overseeing data review staff.

RAVE · EDC