114 jobs for “Biotech Research Scientist”
Isomorphic Labs London
Lead the hardening and scaling of an inference platform serving fleets of cutting-edge ML models for scientific applications. Set strategy and roadmaps, architect next-generation services to solve scaling limits, and partner with research, product and operations teams to align infrastructure with biotech R&D cycles.
Isomorphic Labs London
Lead all externalised drug discovery and preclinical lab operations, building and scaling a global CRO infrastructure for an AI-first drug design platform. Oversee experimental throughput, data QC and turnaround times, embed data-generation-by-design standards, and manage vendor governance, budgets and a team of CRO Scientific Leads, Operations Managers and Compound Managers.
GSK London
Builds and maintains financial and operational models, forecasts and dashboards that guide R&D portfolio and investment decisions, including NPV/rNPV, scenario and sensitivity analysis and Monte Carlo simulation. Works with the Head of Data Science and the Finance Portfolio Analytics Manager, turning scientific, clinical, financial and operational data into clear outputs for review discussions.
GSK USA - Pennsylvania - Upper Providence
Builds and maintains financial and valuation models (NPV/rNPV, scenario and sensitivity analysis) and portfolio forecasts, metrics and KPI dashboards for R&D investment decisions. Runs probabilistic and Monte Carlo simulations, cleans data from scientific, clinical, financial and operational sources, and prepares decision materials for portfolio reviews. Works with the Head of Data Science and the Finance Portfolio Analytics Manager in a hybrid, high-visibility team.
CSL Waltham, United States
Leads an integrated quality assurance organisation covering Good Clinical Practice and Good Pharmacovigilance Practice, reporting to the Head of Global R&D Quality. Sets strategy, operating model and standards for risk-based QA oversight from trial design through close-out, including inspection readiness, CAPAs and clinical safety interfaces such as SAE reconciliation and expedited reporting. Hybrid role with global team leadership and international travel.
CSL Opfikon, Switzerland
Leads strategic sourcing and evaluation of late-stage external clinical assets in Immunology, from Phase 2 through marketed drugs. Sits on the Therapy Area Leadership Team, co-leads New Product Opportunity reviews, engages external KOLs and investigators, and drives cross-functional due diligence with BD to close deals.
Recursion New York, United States US$151,800 – US$220,660 pa
Integrate phenomics, transcriptomics, genomics and proteomics data to nominate novel targets and validate immunology and inflammation disease biology, piloting new methods for target discovery and early patient population hypotheses. Partner cross-functionally with biologists, chemists, data scientists and engineers to build data packages that drive program milestones and investment decisions.
Recursion New York, United States US$151,800 – US$220,660 pa
Integrates phenomics, transcriptomics, genomics and proteomics data to nominate and validate oncology targets and define precision oncology patient strategies. Partners cross-functionally with biologists, chemists, engineers and translational experts to build target data packages and pilot novel discovery methods, including agentic target packages and mechanism-of-action work.
Autolus London
Designs end-to-end data solutions spanning data integration, data warehousing, master data management, governance and analytics for a biopharmaceutical company. Translates business requirements into data models, data flows and integration patterns, and leads architecture and design reviews across enterprise applications and cloud data platforms.
Vertex Pharmaceuticals London
Leads regional or global regulatory strategy for development programs and marketed products, serving as a regulatory lead and primary contact with health authorities. Manages preparation, submission and approval of regulatory applications, advises teams on approval pathways and expedited routes, and monitors regulatory intelligence to inform strategy.
Newton Colmore Cambridge
Lead the design and development of next-generation drug delivery devices, guiding multidisciplinary teams of engineers, scientists and designers from early-stage concepts through to manufacturable solutions. The role blends hands-on R&D work — concept generation, prototyping, verification planning and risk management — with client-facing consultancy, programme leadership and mentoring of junior colleagues.
Moderna London
Shape global CMC regulatory strategy for an innovative mRNA medicines portfolio, driving international submissions and health authority interactions. Prepare and review CMC sections of regulatory filings, advise Manufacturing and Quality teams, and oversee multiple development programs. An individual contributor role with global reach, working alongside teams using digital and Generative AI tools.
Genomics London
Client-facing programme manager role setting up and embedding a multidisciplinary delivery team around a major pharma partnership, running the integrated delivery plan, milestones, dependencies, risks and resourcing. Coordinates across Science, Data, Engineering, Finance, Legal and People stakeholders, running status meetings, reporting and escalations with the partner. Structured as a six-month engagement with an immediate start.
Moderna Oxford
Lead the technical maintenance and engineering setup of a brand-new Label and Secondary Packaging operation at the Harwell site, from URS and FMEA through commissioning, qualification and validation. Develop preventative maintenance strategies, manage external vendors and build the site maintenance team, working with GMP equipment and digital/AI-enabled engineering tools.
Parexel Harrow
Acts as principal labelling strategist within Global Regulatory Affairs, driving development and maintenance of dCCDS, CCDS, USPI and EU SmPC documents across an assigned product portfolio. Leads Global Labeling Committee reviews of proposed label exceptions and represents labelling on regulatory strategy teams, working with safety, clinical and commercial stakeholders. Home or office based across European locations.
