Biotechnology Jobs

• London
• Hybrid
• US$189,750 – US$316,250 pa
• Director

Leads precision diagnostics strategy for oncology programmes, defining diagnostic requirements for trials and overseeing biomarker selection, assay validation and sample handling. Manages project plans, budgets and timelines while engaging diagnostic companies, clinical labs and vendors, and supporting regulatory submissions. Works cross-functionally with research, clinical, regulatory and commercial teams in a hybrid model.

FDA · EU IVDR · PMDA +2

• Stevenage
• Hybrid
• Director

Leads precision diagnostics strategy for oncology programmes, defining biomarker selection, assay validation and sample collection across multiple assets. Oversees project plans, budgets and regulatory submissions while managing external diagnostic partners and clinical labs. Hybrid role based in Stevenage, relocating to Cambridge by early 2029.

FDA · EU IVDR · PMDA/MHLW Japan +2

• Livingston
• On-site
• Entry level

Assembles clinical trial test kits with specimen collection materials according to protocol, prepares investigator instruction manuals and flowcharts, and packages completed kits with documentation and ancillary supplies for shipment. Monitors inventory levels and alerts supervisors when supplies run low to prevent study delays. Site-based role requiring strong attention to detail and organizational skills.

• Livingston
• Entry level

Performs and documents analytical procedures in a regulated laboratory, running routine data analysis and checking results against tolerances. Prepares data for LIMS upload, supports quality investigations and deviations, and calibrates and maintains lab equipment. Also trains other lab personnel and escalates unusual results to senior staff.

LIMS

• 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

• Groton, United States
• Hybrid · 2–3 days in office
• US$124,400 – US$207,400 pa
• Lead

Leads the strategy, design and lifecycle management of digital clinical supply chain systems for Global Clinical Supply, working with product managers and business SMEs on a 3-5 year roadmap. Drives process and technology integration, system modernisation and retirement, and enterprise-level portfolio prioritisation while reporting progress to senior management. Hybrid role with up to 15% travel.

• Andover, United States
• Hybrid · 2–3 days in office
• US$124,400 – US$207,400 pa
• Lead · manages people

Lead the digital transformation of Pfizer's clinical supply chain systems, overseeing the full lifecycle from concept to decommissioning. Define multi-year product strategies, drive process and technology integration, and guide cross-functional teams to ensure regulatory compliance and efficient delivery of investigational products worldwide.

• United Kingdom
• Hybrid
• Mid-level

Manages end-to-end clinical trial supply chains, developing study-specific plans, coordinating cross-functional teams, and ensuring GxP-compliant distribution and inventory levels. Represents the department externally, mentors junior staff, and drives process improvements within a global clinical supplies team.

Microsoft Office

• United Kingdom
• Remote
• Lead

Supports central comparator sourcing for clinical trials on a client-dedicated FSP team, covering market intelligence, sourcing recommendations, and purchase order execution across EMEA. Acts as an SME on the external comparator landscape, advising on regional and central/local sourcing strategy while escalating quality or temperature issues to the client.

• Harrow
• Hybrid
• Mid-level

Drives strategic impact by developing operational and technical solutions for Early Phase clinical trials, collaborating with Enterprise Accounts, Growth Accounts, Commercial Operations and Strategic Business Units. Contributes to business development from opportunity identification through solution design, bid strategy and client engagement, crafting differentiated value propositions and proposal content. Requires 3-5 years of Early Phase Clinical Trials experience and up to 30% travel.

Clinical Trial Management Systems · Proposal Development Platforms · Enterprise Software Solutions

• Weston-super-Mare
• On-site
• £23 – £24 ph
• Senior
• Temporary

Support the daily operational management of a Clinical Chemistry laboratory, performing routine and specialist testing, result validation, and analyser maintenance. Work with Beckman Coulter DxC700 AU, DxI 800 and DxA Automation Track systems, Remisol middleware and WinPath LIMS, participating in IQC/EQA and ISO 15189 compliance.

Beckman Coulter DxC700 AU · Beckman Coulter DxI 800 · Beckman Coulter DxA Automation Track +2

• Leeds
• Director · manages people

Executive leadership role owning QA and regulatory compliance for the Clinical Pharmacology Services unit, covering CPU operations, GMP pharmacy activities and Phase IB/IIA early-phase trials. Sets risk-based quality strategy, inspection readiness and audit programs, leads global matrixed QA teams and represents the company externally on GCP/GMP matters.

• 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.

• Sheffield
• Remote
• Mid-level

Works within cross-functional clinical development teams on trial design, protocol development, analysis planning and regulatory submissions. Independently programs and quality-controls derived datasets and statistical outputs (tables, listings, figures) in SAS or R, and coordinates project teams while acting as client contact on statistical matters.

SAS · R

• Aberystwyth
• £27,319 – £30,378 pa
• Contract

Supports a Wellcome-funded schistosomiasis drug discovery programme, working within a collaborative team across Aberystwyth, Dundee and UT Southwestern. The role involves in vivo animal work underpinning phenotypic and target-based screening of new chemical entities against parasitic trematode worms.