102 jobs for “Biotech Research Scientist”
GSK Upper Providence 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. Builds and leads a matrix Medicine Development Team spanning clinical development, immunology, manufacturing, regulatory, safety, medical affairs and commercial, and drives strategy, go/no-go decisions and lifecycle planning.
GSK USA - Pennsylvania - Upper Providence 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. Builds and directs a matrix Medicine Development Team spanning clinical development, immunology, manufacturing, regulatory, safety, medical affairs and commercial, and drives strategy, go/no-go decisions and lifecycle planning.
Pfizer Cambridge, United States US$176,600 – US$294,300 pa
Leads global evidence generation and health economics and outcomes research for a rare disease therapy, designing HEOR studies, economic models and value dossiers to support reimbursement and patient access. Works within a cross-functional matrix team and with country teams, guiding clinical trial design and payer-facing evidence strategy.
Pfizer Collegeville, United States US$176,600 – US$294,300 pa
Leads the global evidence generation strategy for a rare disease therapy, overseeing HEOR studies such as network meta-analyses, economic models, and non-interventional research from concept to publication. Partners with cross-functional teams and country affiliates to develop value dossiers and patient-reported outcome strategies that support reimbursement and market access. The role sits within Pfizer's HV&E team and involves managing external research collaborations and vendor relationships.
Newton Colmore Spain
Bridge process biology and advanced sensing by running suspension CHO/HEK293 cultures from bench to pilot scale, building Raman/PLS chemometric models, and translating bioreactor behaviour into requirements for engineering and software teams. Work in a multidisciplinary group developing AI-driven bioprocessing systems for mammalian cell culture and monoclonal antibody production, with direct access to the CEO and CTO.
CSL Maidenhead
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 clinical safety interfaces, inspection readiness and CAPA frameworks. Hybrid role with global scope and international travel.
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.
Recursion Remote Opportunity - United Kingdom £136,500 – £167,200 pa
Lead clinical pharmacology and pharmacometrics strategy across a portfolio of rare disease and oncology programs, serving as the clinical pharmacology lead for regulatory interactions and study design from Phase 1-3. Perform and oversee modeling and simulation with tools such as WinNonlin, Monolix, NONMEM and R, and author regulatory sections for IBs, INDs and NDAs. Part of a Pharmacometrics team spanning clinical pharmacology, pharmacometrics and translational modeling, working end-to-end across discovery and development.
Isomorphic Labs Cambridge, United States
Lead and execute the translational medicine strategy for an oncology portfolio, ensuring clinical biomarker assay readiness and data delivery to inform mechanism of action, resistance and future indications. Serve as a core program team member and cancer biology expert, collaborating with AI and computational biology teams to build innovative biomarker analysis tools and advance companion diagnostics.
Recursion Salt Lake City, United States US$200,000 – US$220,500 pa
Lead a team of computational biologists in early discovery, acting as a player-coach who balances hands-on analysis with mentorship. Integrate phenomics, transcriptomics, genomics and proteomics data to nominate oncology and immunology targets, define validation criteria and precision medicine strategies, partnering with biologists, engineers and translational experts.
AstraZeneca London
Finance lead for a designated disease area with full P&L ownership across UK & Ireland in-line and pipeline assets. Drives strategic planning, budgeting, monthly forecasting and pricing/reimbursement business cases, applying AI and advanced analytics, while partnering Commercial, Medical, Market Access and Global Finance. Office-based in London with at least 60% attendance.
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, experimental design, verification planning and risk management — with client-facing consultancy, programme leadership and mentoring of junior colleagues.
Moderna London
Leads CMC regulatory strategy for global submissions including IND, CTA, BLA and MAA, and oversees agency correspondence and compliance for mRNA products. Reviews submissions for readiness, drives health authority interactions, and advises manufacturing and quality teams on change controls and regulatory guidance across vaccines, oncology and rare disease programmes.
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.
