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.

• Oxford
• On-site
• Entry level
• Permanent

Supports the smooth operation of research laboratories through cleaning, equipment maintenance, calibration and inventory management of reagents and consumables. Acts as point of contact for external servicing visits, handles and transports biological samples, and helps maintain health and safety compliance including waste disposal and temperature-sensitive storage.

• Liverpool
• Director · manages people

Leads the Operational Excellence function at a major influenza vaccine manufacturing site, deploying Lean, Six Sigma and the CSL Operating System to translate strategy into operational priorities and financial benefits. Owns the site management system, structured problem solving and continuous improvement, coaching senior leaders and leading the OE team. Reports to the Manufacturing Site Lead and sits on the Site Leadership Team.

CSL Operating System

• Waltham, United States
• On-site
• US$150,975 – US$251,625 pa
• Mid-level

Key member of the Clinical Development team contributing to the design, execution, analysis and reporting of clinical studies across all phases. Works cross-functionally with Medical Monitoring, Clinical Operations, Biostatistics, Data Management and Regulatory Affairs, reviewing safety, efficacy, biomarker and PK/PD data and supporting CSRs and regulatory submissions. Based on-site in Waltham, MA or London, UK.

• London
• On-site

Contributes to the design, execution, analysis and reporting of hepatology clinical studies across all development phases, working with clinical operations, biostatistics, data management and regulatory affairs. Reviews safety, efficacy, biomarker and PK/PD data, supports protocol and CSR development, and engages with investigators and sites. Based on-site in London or Waltham, MA.

• Barcelona, Spain
• Hybrid
• €63,600 – €118,000 pa
• Lead · manages people

Lead and develop a team of Central Monitors, shaping central and site monitoring strategies across a global development portfolio. Oversee trial-data surveillance, risk reviews and signal detection using Central Monitoring technology, translating complex risk signals into actionable insights for Clinical Trial Teams. Partners with clinical, data and risk-surveillance teams to strengthen risk-based monitoring and Risk-Based Quality Management.

Artificial Intelligence

• Harrow
• Remote
• Lead · manages people

Acts as functional lead on the core project team, driving site identification and country selection for clinical trials from award onwards. Designs protocol-specific site questionnaires, leads local teams through surveys, models enrolment scenarios, and presents data-driven strategies to sponsors. Also serves as SME for feasibility systems and may lead stand-alone feasibility studies.

• Sheffield
• Remote
• Lead

Configures, tests and maintains electronic Clinical Outcome Assessment studies in platforms such as Medidata Designer eCOA, translating protocols and licensed instrument requirements into questionnaires, schedules and branching logic. Acts as technical contact for sponsors and vendors, coordinates eCOA-to-EDC integration and deployment, and mentors less-experienced study designers across multiple global trials.

Medidata Designer eCOA · Medidata Rave

• Newcastle upon Tyne
• On-site
• Senior

Leads and coordinates global field action management across Leica Biosystems, including recalls, corrections, removals and Field Safety Corrective Actions. Acts as global process owner and subject matter expert, partnering with Quality, Regulatory, Operations and Commercial teams on investigations, risk assessments and vigilance reporting. Also drives inspection readiness, KPI monitoring and continuous improvement across regions.

EU IVDR · ISO 13485 · FDA +1

• Leeds
• On-site
• Senior

Lead early-phase clinical trials as Principal Investigator or Project Physician, taking studies from start-up through closeout and the Clinical Study Report. Work across first-in-human studies, multiple therapeutic areas and an NHS Trust collaboration, with on-call cover and mentoring of less experienced physicians.

MHRA · cGMP · NHS Trust

• Uxbridge
• Director · manages people

Owns the clinical strategy for one or more neuropsychiatry programs, serving as Clinical Trial Physician and clinical point of accountability for the Clinical Development Team. Leads trial design, data interpretation, regulatory submissions and health authority interactions, with matrix leadership across global scientific teams.

• Livingston
• Hybrid
• Mid-level

Coordinates laboratory study setup for a clinical research organisation, covering protocol and budget review, database setup, project plans, timelines and documentation. Presents protocol materials at kick-off and investigator meetings, manages scope changes and budget monitoring, and works with project management to improve processes across global Phase I-IV trials.

• London
• Lead

Lead the development of country, site and patient enrollment strategies for complex global clinical trials, analysing clinical and operational data to shape feasibility and study delivery. Present recommendations to clients and senior stakeholders, with a particular focus on APAC opportunities including China. Mentors colleagues and acts as subject-matter expert for planning tools.

• Oxford
• On-site
• Senior

Hands-on sole contributor owning equipment uptime and reliability in a new GMP manufacturing facility, acting as technical escalation point for technicians and contractors. Leads structured troubleshooting, RCA, CAPA ownership, CMMS data integrity, preventative maintenance planning and small capital projects, working closely with Engineering and QA. Supports 24/7 operations across early, mid and occasional night shifts with callouts, applying Lean/6S, RCM, FMEA and digital-first approaches.

CMMS · Maximo · SAP PM +5

• 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