Biotechnology Jobs

Isomorphic Labs · Cambridge, United States

Lead in vitro and cellular pharmacology strategy for small-molecule drug design programs, defining screening cascades and guiding biophysical, biochemical and cell-based assays from hit identification to candidate selection. Bridge computational AI/ML predictions with laboratory validation, managing CRO partnerships and collaborating with chemistry, structural biology and translational teams.

Isomorphic Labs · Cambridge, United States

Designs and implements translational strategies for small molecule oncology and immunology programs, from early discovery through candidate selection and clinical phase. Oversees CRO activities, PK/PD and safety assessments, and biomarker strategies, bridging computational predictions with laboratory validation. Some roles include managing 2-3 in vivo pharmacologists.

EMBL-EBI · Saffron Walden

Develops FAIR infrastructure connecting proteomics evidence (XL-MS, CF-MS, AP-MS) with structural restraints, predicted structures and integrative models. Builds data models, APIs, conversion and validation tools with PRIDE and wwPDB, extending community standards for structural interactomics and linked deposition workflows.

EMBL-EBI · Saffron Walden · £3,452 – £3,861 pm

Develops and maintains Python and Java data pipelines for ChEMBL releases, plus other chemogenomics services like SureChEMBL, UniChem and ChEBI. Involves cheminformatics tooling (RDKit, Open Babel, InChI, SMILES), SQL databases, Linux and Git-based workflows, with cross-team work on data quality and integration of external resources such as PubChem and BindingDB.

GSK · London · £123,000 – £205,000 pa

Leads respiratory epidemiology and real-world evidence programmes that inform vaccine development, designing and overseeing complex studies on disease burden, treatment patterns and safety. Partners with clinical development, safety, regulatory and external collaborators, and mentors junior staff. Requires deep RWE and pharmaco-epidemiology expertise in a global, matrixed environment.

GSK · Wavre, Belgium · €123,000 – €205,000 pa

Leads respiratory epidemiology and real-world evidence programs that inform vaccine development, owning the epidemiology plan for at least one asset or disease area. Designs and oversees complex observational studies using claims, EHR and registry data, advises clinical, safety and regulatory teams, and manages external partnerships while mentoring junior scientists.

Vertex Pharmaceuticals · London

Join the International Nephrology marketing team for a 12-month industrial placement, supporting commercial launch strategies for a potential rare kidney disease medicine. You'll work cross-functionally on tactical marketing plans, build product and disease knowledge, and manage vendors and budgets, gaining hands-on pharma launch experience.

Vertex Pharmaceuticals · London

A 12-month industrial placement within an international Medical Affairs team, supporting the planning and execution of medical projects in assigned therapeutic areas. The role involves project management, monthly dashboard reporting, managing external agencies, monitoring budgets for medical education events and advisory boards, and liaising with cross-functional and external stakeholders.

IQVIA · Cambridge

Hands-on bioanalytical role developing, optimising and running LC-MS/MS assays for small and large molecule DMPK studies in an early discovery setting, analysing matrices such as plasma, blood, brain, bile, faeces and urine. Combines complex mass spectrometry troubleshooting and method development with leading scientific projects, mentoring colleagues and driving novel assay innovation in a matrix team.

Ipsen · London

Leads one or more Early Development Asset Teams, owning integrated strategy from candidate nomination through first-in-human trials across preclinical, translational, clinical, regulatory and CMC workstreams. Serves as scientific champion for oncology assets, presenting data and investment recommendations to governance bodies and contributing to in-licensing due diligence.

Ipsen · London

Leads global operational delivery of early development oncology programs, managing Clinical Project Managers, Monitoring Leads and CTAs. Owns the clinical development plan, CRO and site selection strategy, budgets and timelines, and serves on Asset Teams. Requires deep first-in-human and Phase I oncology trial expertise.

Fortrea · Maidenhead

Monitors clinical trials across the UK under a risk-based model, covering oncology and haematology studies plus neuroscience, cell and gene therapies and other therapeutic areas. Requires at least six months of independent monitoring experience and involves 8+ on-site days per month, working with multiple protocols for biotech and biopharma sponsors.

Pfizer · New York, United States · US$176,600 – US$294,300 pa

Leads global evidence generation strategy for a rare disease therapy, overseeing HEOR studies such as network meta-analyses, economic models, and patient-reported outcomes. Partners with cross-functional teams and country affiliates to support reimbursement and market access, managing vendors and budgets. Requires deep HTA and health economics expertise within a matrix organization.

Pfizer · Europe - Any Pfizer Site · US$176,600 – US$294,300 pa

Leads global health economics and outcomes research for a rare disease asset, developing evidence generation strategy and HEOR studies such as network meta-analyses, economic models and patient-reported outcomes. Oversees launch deliverables including value dossiers and systematic literature reviews, working with cross-functional and country teams to support reimbursement and patient access.

Randstad Construction & Property · London

Manages a portfolio of clinical research studies end to end, leading cross-functional teams and client relationships for Patient Cloud products such as eCOA/ePRO, eConsent and virtual trials. Involves risk assessment, study documentation and milestone tracking, with flexibility needed to work American time zones.