539 jobs for “Research Scientist”
GSK Zug, Switzerland US$189,750 – US$316,250 pa
Serves as the physician within an oncology clinical program team, leading medical monitoring and safety oversight for genitourinary cancer studies. Interprets clinical and safety data, contributes to protocol development and regulatory interactions, and acts as a core member of the Clinical Matrix Team. Hybrid role requiring on-site presence at least two days per week.
GSK Waltham, United States US$189,750 – US$316,250 pa
Serves as the physician within a clinical program team, leading medical monitoring and safety oversight for genitourinary oncology studies. Interprets clinical and safety data, contributes to protocol development and regulatory interactions, and acts as a core member of the Clinical Matrix Team. Hybrid role requiring on-site presence at least two days per week.
TRS Consulting Telford £43,000 pa
Servicing, installing, repairing and calibrating sophisticated laboratory and scientific X-ray systems on customer sites across pharmaceutical and research environments. Requires a field service or technical support background with electronics qualifications and experience on high-value capital equipment; full product training is provided.
TRS Consulting Shropshire £43,000 pa
Servicing, installing, repairing and calibrating sophisticated laboratory and scientific X-ray systems on customer sites across pharmaceutical and research environments. The role suits a field service or technical support engineer with electronics qualifications and experience of high-value capital equipment, with full product training provided.
CSL Opfikon, Switzerland US$212,000 – US$251,000 pa
Leads the full statistical contribution to a clinical development programme, defining statistical strategy for trial design, analysis and regulatory submissions, and representing Biostatistics in interactions with the FDA, EMA and PMDA. Also manages outsourcing to CROs and internal statistical programmers, and supports departmental improvement initiatives.
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.
Ipsen London
Leads global cross-functional teams to plan, coordinate and deliver regulatory submissions such as new marketing authorisations and new indications. Manages integrated submission timelines, scenario planning, risk mitigation and forecasting, working with Regulatory Affairs, Clinical, Quality and Manufacturing. Requires CTD/eCTD filing expertise and project management tools in a global matrix environment.
Ipsen London
Leads global cross-functional teams to plan, coordinate and deliver regulatory submissions for new marketing authorisations, new indications and other major filings. Manages integrated submission timelines, scenario planning, risk mitigation and forecasts, working with Regulatory Affairs, Clinical, Quality and Manufacturing under the CTD/eCTD framework.
Johnson & Johnson Innovative Medicine Maidenhead
Leads the preparation and finalisation of clinical documents within the Regulatory Medical Writing team, supporting the Immunology therapeutic area. Takes a lead role on assigned projects for content, scientific strategy, timing and tracking, and manages direct reports including hiring, goal-setting and development. Involves guiding cross-functional teams, peer review and maintaining knowledge of ICH and regulatory guidelines.
Moderna London
Shapes and executes a UK-wide government affairs strategy as a sole contributor, focusing on respiratory vaccines and building relationships across government, Parliament and industry. Involves legislative and regulatory analysis, trade association management, and exploring Generative AI for policy intelligence, working with Communications, Medical and Market Access teams.
Danaher Newcastle upon Tyne
Provides medical and clinical leadership for the development of novel diagnostic and companion diagnostic assays and platforms supporting precision medicine. Acts as subject matter expert for R&D projects, clinical studies and regulatory submissions, and supports pharma partnerships and pathology education. Hybrid role based in Newcastle Upon Tyne with 30-40% international travel.
Johnson & Johnson Innovative Medicine High Wycombe
Independent clinical quality-risk leadership role translating risk signals into proactive mitigation, escalation and inspection readiness across trials and programs. Involves maintaining Clinical Quality Plans, driving risk monitoring reviews, advising on CAPA plans, and leading pre-submission quality portfolio reviews and mock inspections. Combines hands-on risk ownership with cross-functional influence and coaching of team members.
EMBL-EBI Saffron Walden
Lead solution architecture for digital experience initiatives spanning web applications, APIs, content platforms and AI-enabled services, remaining hands-on through discovery, prototyping and architectural development. Bridge UX and engineering, translating user needs into accessible, sustainable architectures while providing technical direction and people management to the development team. Focus on LLMs, retrieval-augmented generation, agents and semantic search.
Loughborough University Loughborough
A research post investigating the biological mechanisms behind fatigue and post-exertional symptom exacerbation in Long COVID and related post-infectious conditions. Day-to-day work covers participant recruitment, cardiopulmonary exercise testing, autonomic assessments, wearable deployment, biological sample collection and processing, data management and project coordination, in collaboration with Imperial College London and international partners.
University of Cambridge Cambridge £38,448 – £46,970 pa
Primarily experimental wet-lab postdoc developing programmable nucleic-acid systems that sense defined human genomic sequences and convert molecular recognition into engineered DNA outputs, with applications to genetic privacy. Based in the Department of Genetics, the role involves hands-on design, construction and troubleshooting of novel molecular systems plus quantitative analysis of assay performance to guide experimental iterations.
