Biotechnology Jobs

GSK · Stevenage · US$222,750 – US$371,250 pa

Serves as the physician within an oncology clinical programme team, leading medical monitoring, safety oversight and clinical data interpretation for GI studies. Partners with a Senior Scientist and cross-functional matrix teams on protocol development, regulatory interactions and investigator engagement. Requires on-site presence 2-3 days a week, with the Stevenage base relocating to Cambridge, UK by early 2029.

GSK · USA - Pennsylvania - Upper Providence · US$242,550 – US$404,250 pa

Senior physician leader providing medical oversight, safety monitoring and clinical insight across lung cancer studies, from protocol design through data interpretation. Serves on the Clinical Matrix Team, contributes to regulatory interactions and external scientific engagement, and mentors Medical Directors within the programme. Requires deep lung cancer drug development expertise, including early phase trials.

Fortrea · Maidenhead

Supporting complex oncological clinical trials, this client-dedicated role involves tracking study activities, maintaining essential documentation and regulatory compliance, managing Trial Master File documentation and quality control, and liaising with vendors and coordinating study supply shipments. It also covers site and study material preparation, meeting coordination and minute-taking, plus general administrative and systems support within a project team.

IQVIA · Reading

Shapes and drives end-to-end clinical trial supply strategy, translating study protocols into kit designs, demand forecasts and packaging plans. Oversees vendors, IRT systems, distribution and temperature-excursion management while leading client and vendor meetings. Combines analytical planning with operational leadership across GxP-regulated clinical supply work.

Fortrea · Maidenhead

Conducts and oversees site monitoring visits, managing site initiation, monitoring and closeouts while ensuring patient safety, data integrity and GCP compliance. Supports feasibility assessments, investigator recruitment and vendor coordination, and mentors junior team members. Requires Phase I patient-study experience within a client-dedicated FSP team.

Ipsen · London

Drives clinical supply forecasting and budgetary requirements for global clinical programmes, translating study protocols and recruitment projections into forecasting tools and consolidated IMP estimates. Monitors forecast evolution, analyses deviations and proposes mitigation plans, coordinating with manufacturing, packaging, procurement and distribution teams to prevent stock-outs. Operates in a highly matrixed environment, leading IMP kick-off and estimation meetings and supporting continuous improvement and GMP compliance.

Parexel · Sheffield

Leads research design and analytical strategies for clinical trials, developing and reviewing statistical analysis plans and authoring reports, abstracts and manuscripts. Acts as functional lead on study teams, directing biostatistical activities, performing complex analyses in SAS or R, and quality-controlling deliverables while mentoring junior staff and liaising with clients on scope and budget.

Novartis · Barcelona, Spain · €63,600 – €118,000 pa

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.

IQVIA · Reading

Leads strategic planning, oversight and delivery of a portfolio of clinical supply chain projects, ensuring timely provision of trial supplies across global studies. Day to day this covers protocol interpretation, label text, demand forecasting, packaging campaigns, IRT system setup and vendor oversight, plus temperature excursion and risk management. Distinct for its global, client-facing scope and process improvement focus.

University of East Anglia · Norwich · £21,805 pa

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.

University of East Anglia · Norwich · £21,805 pa

A four-year PhD project using engineering biology to develop bacterial and human ferritin nanocages for encapsulating small molecules, peptides and proteins, with applications in biocatalysis and therapeutics. The work spans protein purification, bioanalytical methods, spectroscopy, mass spectrometry and microscopy, targeting enzymes such as hydrogenase and targeted molecular delivery. Based in the Le Brun lab at UEA's School of Chemistry, Pharmacy and Pharmacology.

AstraZeneca · London

Hands-on health economics role leading the delivery of cost-utility and budget impact models in Excel and VBA for national HTA submissions to NICE, SMC and AWMSG. Partners with UK Market Access, Medical and Brand teams plus the global HEOR function, and also builds early cost-effectiveness models for future brands and indications.