Biotechnology Jobs

• London
• Hybrid · 2 days in office
• Director · manages people

Leads the scientific strategy and operational execution of global implementation science studies, designing mixed-methods research using frameworks such as CFIR and RE-AIM to generate real-world evidence for HIV products. Oversees data analysis, study reports, publications and dissemination, while managing external vendors, budgets and cross-functional partners. Also mentors team members and represents implementation science in global evidence-generation forums.

CFIR · RE-AIM

• Durham, United States
• Lead

Lead authoring and strategic planning for clinical and regulatory documents, including protocols, clinical study reports, briefing documents and submission dossiers. Manages end-to-end writing projects, coordinating contributors, timelines and quality checks, and acts as subject matter expert on medical writing standards, CTD structure and regulatory expectations while driving process improvement and audit readiness.

• London
• Hybrid
• Mid-level

Drives country-level clinical trial execution, owning study start-up, site budget negotiation, Clinical Trial Research Agreements, and regulatory/IRB submissions. Acts as the link between investigator sites, regulators, and internal teams to keep trials launch-ready and compliant with ICH/GCP. Also mentors CRAs and CTCs and leads process improvement projects.

Clinical Management Systems

• Manchester
• Senior

Monitors clinical trial sites across selection, initiation, monitoring and close-out visits in line with GCP, while driving subject recruitment and tracking regulatory submissions, CRF completion and data query resolution. Also trains site staff, maintains TMF/ISF documentation and may support site financial management and start-up activities.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• Reading
• Senior

Monitors clinical trial sites across the UK, performing selection, initiation, monitoring and close-out visits in line with GCP and sponsor requirements. Tracks recruitment, regulatory submissions, CRF completion and data queries, and maintains TMF/ISF documentation. Dedicated to a single sponsor within IQVIA's cFSP model.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint +2

• Ireland
• On-site
• Mid-level · manages people
• Permanent

Manages the people, resources and performance of a 4-on-4-off laboratory shift, owning KPIs such as productivity, error rates, QC pass rate, instrument downtime and sample backlog. Acts as incident lead and primary escalation point for Shift Leads, coordinating with Clinics, Customer Support, IT and Quality to keep testing accurate and within turnaround time.

Microsoft Word · Microsoft Outlook · Microsoft Excel +2

• Ireland
• On-site
• Senior · manages people
• Permanent

Lead the end-to-end performance of a 24/7 regional clinical laboratory in Sandyford, Dublin, managing turnaround times, QC, repeat rates, stock control and cost efficiency. Oversee Team Leads, drive continuous improvement with data, and maintain compliance with ISO 17025, ISO 15189, GCP and MHRA standards while writing SOPs and work instructions.

Microsoft Excel · Microsoft Outlook · Microsoft Word +1

• Harrogate
• Entry level

Trainee role performing routine macroscopic necropsy techniques, including trimming and retaining organs across a wide range of species, plus animal handling and euthanasia. Involves precise sample labelling, accurate data recording, reagent preparation and some out-of-hours or weekend cover once trained, in a physical, fast-paced laboratory environment.

• Harrogate
• Entry level

Trainee role in a purpose-built histology lab, trimming and processing animal tissue samples, performing microtomy, staining and microscopic quality control. Work follows Good Laboratory Practice with cross-training in necropsy, using automated processing and motorised microtomes in a fast-paced production environment.

Automated Tissue Processors · Motorised Microtomes

• Sheffield
• £39,560 – £48,337 pa
• Entry level
• Contract

Lead the design, assembly and clinical validation of a novel dialyser prototype within the Thermofluids Group, testing with blood-mimicking fluids and human blood to assess cleaning efficiency, clotting risk and biocompatibility. Work alongside two other Research Associates covering numerical simulation and experimental fluid dynamics, in collaboration with the Medical School and Sheffield Teaching Hospitals.

• London
• Hybrid
• Director

Leads scouting, evaluation and onboarding of external partnerships focused on computational drug discovery, especially AI/ML and physics-based molecular design. Runs technology landscape reviews, manages a portfolio of assessment projects, and negotiates contracts with partners while bridging internal and external scientists.

• 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

• London
• £60,000 – £75,000 pa
• Senior · manages people

Lead the UK scientific affairs strategy for an international probiotic and functional food organisation, acting as senior scientific authority. Build KOL relationships across academia and healthcare, oversee human studies and research, ensure claims meet regulations, and manage a scientific affairs team while collaborating with European and global colleagues.

• London
• Hybrid
• Senior
• Permanent

Drive innovation as a strategic consultant on high-impact drug discovery projects with external pharma and biotech partners. Navigate the full development pipeline from target discovery to patient stratification, applying statistical human genetics and large-scale genomic data analysis in R or Python. Partner-facing role translating complex findings into actionable insights.

• London
• Hybrid
• Entry level
• Permanent

Early-career scientist role in a Life Sciences team, generating therapeutic hypotheses by mining in-house genomic data with statistical methods to identify and triage drug targets. Also develops and optimises polygenic risk score tools for patient stratification, working with omic data using statistical and AI/ML approaches and communicating findings to internal and external stakeholders.

Git · GitHub · WDL +4