96 jobs for “Biotech Research Scientist”
Mytos London
Owns all aspects of hardware design for automated cell-production machines, from concept through to manufacture, improving robustness and reliability. Leads development of systems interfacing with optics and fluidics, refines test rigs and quality processes, and helps shape engineering culture. Based on-site in the lab at Imperial College's White City innovation hub.
Mytos London
Open general application for a London-based biotech automation company building machines that fully automate human cell production. The team, drawn from ex-Dyson engineers and Nature-published scientists, seeks people with a track record of solving hard technical or non-technical challenges, low ego and high curiosity, including those starting their first job.
Isomorphic Labs London
Contribute to the design of novel large-molecule therapeutics by applying computational and machine learning methods to predict biologics properties such as affinity, developability and immunogenicity from sequence. Work within an interdisciplinary computational sciences team alongside ML and biologics discovery experts, benchmarking models, analysing lab data and shaping data-generation strategies for active learning.
Isomorphic Labs London
Lead pharmacology and translational biology strategy for large molecule therapeutics, designing in vivo efficacy and complex in vitro functional assays. Act as Biology Lead on projects, coordinating internal workflows and external CROs, and collaborate with ML and computational biology teams to feed data into generative AI design loops.
GSK London US$340,500 – US$567,500 pa
Leads global development of a cancer vaccine asset from late-stage transition through approval and launch, acting as single point of accountability and chairing a cross-functional matrix Medicine Development Team spanning clinical, translational, regulatory, manufacturing and commercial. Drives strategy, go/no-go decisions and lifecycle plans for novel vaccine platforms such as mRNA and neoantigen-based therapies.
GSK Waltham, United States US$340,500 – US$567,500 pa
Leads global development of a cancer vaccine asset from late-stage transition through approval and launch, acting as single point of accountability across major markets. Builds and directs a matrix Medicine Development Team spanning clinical development, immunology/biomarkers, manufacturing, regulatory, safety, medical affairs and commercial, and represents the asset to senior governance boards.
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.
Vertex Pharmaceuticals London
Leads the development and execution of international regulatory strategy across European and Rest of World markets, from first-in-human through post-marketing. Represents Global Regulatory Affairs on core development teams, manages project plans and resources, and advises senior management. Also a people manager within the International GRA leadership team, driving process improvement and regulatory policy engagement.
Relation Therapeutics London
Senior project manager role coordinating a multi-year osteoporosis drug discovery programme across target ID, hit-to-lead, lead optimisation and candidate selection. Involves orchestrating matrixed wet lab, ML, data science and engineering teams plus CROs, managing plans, budgets, risks and governance, and translating scientific objectives into integrated timelines and milestones.
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.
Danaher Portsmouth
Responsible for new product development and improvement projects for hardware and disposable devices used in the biotech industry, taking initiatives from spec definition through design, testing and validation to manufacturing transfer. Provides technical leadership on complex engineering challenges, applies 3D CAD design, manages project plans and resources, and reports progress to leadership. On-site role with up to 20% international travel.
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.
