86 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.
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.
CSL Maidenhead
Leads strategic sourcing and evaluation of late-stage external clinical assets in Immunology, from Phase 2 through marketed drugs, as the senior S&E leader within the Therapy Area Leadership Team. Drives proactive sourcing, cross-functional due diligence, and KOL engagement, partnering with BD to advance high-priority opportunities through negotiation and deal close.
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 Remote Opportunity - United States US$261,800 – US$346,060 pa
Lead clinical pharmacology and pharmacometrics strategy across a portfolio of rare disease and oncology programs, serving as the clinical pharmacology lead and regulatory representative. Oversee modeling and simulation (population PK, PK-PD, exposure-response) and provide pharmacology input on Phase 1-3 study designs. Work cross-functionally with clinical, translational and discovery teams in an end-to-end drug development environment.
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.
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.
Relation Therapeutics London
Develops and benchmarks machine learning models for DNA sequence, regulatory elements and genetic variation, including variant effect prediction and representation learning. Integrates sequence-derived representations with transcriptomic, epigenomic and perturbational data to uncover disease mechanisms and support target prioritisation, working within the interdisciplinary Rosalind team.
Autolus US - East Coast
Leads identification, evaluation and execution of strategic partnerships, licensing, M&A and co-development deals, from sourcing through due diligence, structuring and closing. Represents the company to biotech, pharma and academic partners, monitors competitive and market dynamics, and advises executive leadership on external innovation strategy post-launch.
Isomorphic Labs Cambridge, United States
Lead end-to-end clinical trial material planning, vendor management, packaging, labeling, inventory and global distribution for an AI-first drug discovery company. Act as the clinical supply authority within a lean Pharmaceutical Sciences & CMC team, building scalable systems and vendor networks while partnering closely with Clinical Operations and CROs.
Vertex Pharmaceuticals London
Oversees cell and gene therapy Contract Manufacturing Organizations as the primary on-site point of contact, providing operational, quality and technical oversight of cGMP commercial supply. Acts as a Person-in-Plant and SME within the Virtual Plant Team, managing deviations, change controls, batch data and supplier governance, with up to 50% travel and shift coverage for critical process steps.
