Biotechnology Jobs

• London
• Hybrid · 3–4 days in office
• Senior

Shapes and executes a UK-wide government affairs strategy as a sole contributor, focusing on respiratory vaccines and building relationships across government, Parliament and industry. Involves legislative and regulatory analysis, trade association management, and exploring Generative AI for policy intelligence, working with Communications, Medical and Market Access teams.

Generative AI

• Oxford
• On-site
• Senior

Leads the creation, review and oversight of investigator site budgets and grants across Phase I–IV clinical trials, using Grants Manager/GrantPlan and FMV benchmarking. Manages CRO site budget and CTA negotiations, scenario planning and site activation timelines, with exposure to Generative AI tools for analytics.

Grants Manager · GrantPlan · MS Office +1

• Opfikon, Switzerland
• Hybrid · 3 days in office
• US$212,000 – US$251,000 pa
• Director

Leads the full statistical contribution to a clinical development programme, defining statistical strategy for trial design, analysis and regulatory submissions, and representing Biostatistics in interactions with the FDA, EMA and PMDA. Also manages outsourcing to CROs and internal statistical programmers, and supports departmental improvement initiatives.

SAS · R

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

Designs and troubleshoots experiments in continuous evolution, engineering orthogonal replication systems for targeted gene evolution while preserving host viability. Involves computational analysis of complex datasets, publishing high-quality research, mentoring junior staff, and pursuing IP and translational opportunities within a new Oxford institute.

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

Designs and troubleshoots experiments in synthetic chromosome engineering, including centromere design, mitotic segregation and meiotic recombination in mammals and plants. Involves large DNA construct assembly, cell culture, NGS, live-cell imaging and FISH, plus computational analysis, publishing, mentoring junior researchers and pursuing IP and translational opportunities.

NGS

• Maidenhead
• Senior

Acts as case management subject matter expert for assigned clinical trials, overseeing safety reporting plans, vendor performance and ICSR compliance. Leads pharmacovigilance processes, supports GxP inspections and audits, and provides study-specific training to vendors and internal teams. Requires deep PV and regulatory knowledge in a multinational pharmaceutical setting.

Drug Safety Database

• London
• Hybrid
• £67,900 – £126,100 pa
• Senior

Co-leads cross-functional Clinical Trial Teams and global studies from planning through close-out, managing timelines, budgets, risks and inspection readiness. Partners across global and local functions on recruitment, data operations and vendor performance, while championing operational excellence and continuous improvement.

• Barnard Castle
• Contract

Support a secondary manufacturing site's production area with technical services including new product introduction, troubleshooting, and technical projects. Design and validate manufacturing processes, drive improvements using lean and Six Sigma, and lead FMEAs, risk assessments and change controls under cGMP and EHS standards.

• London
• Director

Provides scientific and medical expertise at study level across early- and late-phase hepatology assets, serving as medical monitor for Phase 1–4 trials and leading protocol, IB, ICF and CSR authoring. Works within cross-functional global study teams and the Clinical Matrix Team, integrating efficacy, safety and biomarker data to inform asset and portfolio decisions, with informal coaching of less experienced clinical scientists.

• London
• Hybrid
• £63,917 – £118,703 pa
• Director

Acts as a QA liaison between clinical trial teams and third parties, providing expert support through due diligence, qualification, governance and ongoing monitoring. Focuses on technology-enabled vendors such as digital health tools, medical devices and AI, covering risk assessment, audit support, inspection readiness and escalation of quality issues.

DHT · SaMD · SaaS +1

• Wolverhampton
• Mid-level · manages people
• Permanent

Responsible for managing a pathology laboratory's day-to-day operations, ensuring compliance with ISO 17025, UKAS and retail quality standards. Duties include safety and COSHH compliance, equipment calibration, audit leadership, KPI monitoring, and developing Team Leaders while maintaining 7-day shift coverage.

LIMS · Microsoft Excel · Microsoft Word

• Guildford
• Mid-level
• Permanent

Hands-on laboratory role analysing pharmaceutical samples including APIs, medicines, herbal products and packaging for MHRA Laboratories. Uses HPLC, GC, GC/LC-MS, IR, Raman, UV, dissolution and wet chemistry, with responsibility for drafting reports, validating data, equipment calibration and maintaining an ISO/IEC 17025 quality system. Works within a team of around 30 analytical scientists, independently coordinating project workloads.

Microsoft Word · Microsoft Excel

• London
• Remote
• Senior

Responsible for the successful delivery of clinical studies at assigned investigator sites, acting as the primary point of contact for site management, monitoring, and study execution. Leads site preparation, initiation, routine monitoring, and close-out, conducting onsite and remote visits, source data review and verification, and CRF review while managing risk-based quality and regulatory compliance. Works within a local study team supporting a key sponsor, with travel across the UK and internationally.

CTMS · eTMF

• London
• Remote
• Senior

Responsible for the successful delivery of clinical studies at assigned investigator sites, acting as the primary point of contact for site management, monitoring, and study execution. Leads site preparation, initiation, routine monitoring, and close-out, conducting onsite and remote visits, source data review and verification, and CRF review. Works within a local study team for a key sponsor, using CTMS, eTMF and risk-based quality management, with travel across the UK and internationally.

CTMS · eTMF

• Leeds
• On-site
• Entry level
• Permanent

Prepare and handle investigational medicinal products in a cGMP clean room, applying sterile technique and GMP during live first-in-human studies. Work in pairs with Technical Officers on study set-up, dose calculations, batch records and equipment checks, with the clinic and pharmacy under one roof at an MHRA-accredited Phase I unit.

Outlook · Word · Excel +1