96 jobs for “Biotech Research Scientist”
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.
GSK London
Provides advanced scientific expertise in safety evaluation and risk management for key oncology assets in clinical development, leading signal detection, benefit-risk assessment and regulatory safety submissions. Represents the Safety Evaluation & Risk Management function on cross-functional clinical matrix and project teams, escalating emerging safety issues to senior governance. Mentors junior staff and partners with Safety Physicians to shape long-term safety strategy.
GSK Poznań, Poland PLN 525,750 – PLN 876,250 pa
Provides advanced scientific expertise in safety evaluation and risk management for key oncology assets in clinical development, leading signal detection, benefit-risk assessment and regulatory safety submissions. Represents SERM on cross-functional clinical matrix teams, escalates emerging safety issues to governance bodies and mentors junior staff within a global matrix environment.
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.
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 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.
Autolus Stevenage
Accountable for onboarding and ongoing performance management of apheresis and treatment centres supporting clinical and commercial CAR T-cell therapies across the UK and Rest of World. Serves as the technical operations single point of contact, conducting site assessments, training centre staff, supporting quality systems and deviations, and managing process change rollouts. Involves up to 50% travel and possible management of contract employees.
SRG Darlington £65,000 – £85,000 pa
Lead multidisciplinary operational teams across two sites, covering operations, engineering, facilities and site services. Drive continuous improvement, GMP and H&S compliance, facilities management, budgets and capital projects supporting biologics, RNA and medicines manufacturing. Senior leadership role shaping facility strategy and operational capability.
Moderna London
Lead CMC regulatory strategy for UK-manufactured and UK-licensed mRNA products across development, registration and post-approval lifecycle. Act as primary point of contact with the MHRA, oversee submissions and manufacturing change assessments, and shape global regulatory approaches across cross-functional matrix teams.
