539 jobs for “Research Scientist”
GSK Stevenage
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 with at least two days per week on-site.
GSK London
Serves as the physician within oncology clinical program teams, leading medical monitoring, safety oversight and clinical data interpretation for genitourinary cancer studies. Partners with the Senior Scientist and cross-functional Clinical Matrix Team on protocol development, investigator engagement and regulatory interactions, with hybrid working of at least two days on-site per week.
Ipsen London
Leads global operational delivery of early development oncology programs, managing Clinical Project Managers, Monitoring Leads and CTAs. Owns the clinical development plan, CRO and site selection strategy, budgets and timelines, and serves on Asset Teams. Requires deep first-in-human and Phase I oncology trial expertise.
University of Sussex Brighton £38,784 – £46,049 pa
Postdoctoral position in Professor Claudio Alonso's lab studying the molecular mechanisms of neural development and function in Drosophila. The fellow will use molecular biology, transcriptomics, neurogenetics, optogenetics, imaging and neurophysiology within a collaborative neuroscience department. Fixed term until 30 June 2028, with possible extension.
SPD Development Company Ltd Bedford £30,000 – £35,000 pa
Supports the set-up, conduct and monitoring of internal clinical studies, covering supply sourcing and shipment, volunteer recruitment, payment administration, source data verification and testing. Maintains inspection-ready documentation and reports study status to the wider clinical team, working to GCP and relevant IVDR/ISO standards.
Fortrea Leeds
On-site CRA role monitoring Phase I–Ib studies inside a 100-bed Leeds Clinical Research Unit, covering pre-study, initiation, routine monitoring and close-out visits. Works alongside clinic, pharmacy and lab teams during first-in-human dosing days, using integrated eSource and EDC systems to focus on data integrity and protocol compliance rather than mechanical SDV.
University of Oxford Oxford £39,424 – £47,779 pa
Develop novel statistical and machine learning methods for large-scale genomic, phenotypic and health data, covering areas such as genomic language models, multimodal and federated learning, and multi-ancestry methods. Implement reproducible research software, apply it to biobank-scale datasets, evaluate statistical and predictive performance, publish findings and guide junior researchers.
MSD London
Lead site performance and compliance for assigned clinical protocols across the South East, acting as primary site contact through all study phases. Conduct remote and on-site monitoring to ICH/GCP standards, manage regulatory documentation in CTMS and eTMF, and mentor junior CRAs. Involves roughly 65-75% domestic and international travel.
Ipsen London
Serves as the clinical trial pharmacy subject matter expert across global oncology programmes, advising on investigational product handling, preparation, storage and accountability, and on hazardous drug and CSTD requirements. Develops pharmacy manuals and training for site pharmacists and study teams, supports audits and CAPAs, and oversees FSP pharmacists and external vendors. Hybrid role spanning London, Paris or Cambridge MA.
Fortrea Maidenhead
Monitors clinical trials across the UK under a risk-based model, covering oncology and haematology studies plus neuroscience, cell and gene therapies and other therapeutic areas. Requires at least six months of independent monitoring experience and involves 8+ on-site days per month, working with multiple protocols for biotech and biopharma sponsors.
Parexel London
Responsible for the successful delivery of clinical studies at assigned investigator sites, acting as the primary point of contact for site management, monitoring, and study execution. Leads site preparation, initiation, routine monitoring, and close-out, conducting onsite and remote visits, source data review and verification, and CRF review. Works within a local study team for a key sponsor, using CTMS, eTMF and risk-based quality management, with travel across the UK and internationally.
University of Sheffield Sheffield £32,722 – £37,369 pa
You will process samples for molecular and genomic analysis, maintain laboratory equipment, and support visiting researchers in a Genomics Laboratory. The role also involves training users new to molecular biology, advising external clients, and contributing to research and development that expands the facility's capabilities.
IQVIA Reading
Monitors clinical trial sites across the UK, handling selection, initiation, monitoring and close-out visits in line with GCP and ICH guidelines. Manages multiple protocols, drives subject recruitment, tracks regulatory submissions and CRF data, and maintains Trial Master File documentation. Based in Reading with regular travel to investigative sites.
Parexel London
Oversees monitoring activities across investigator sites in a sponsor-dedicated model, ensuring protocol compliance, data integrity, patient safety and inspection readiness. Conducts remote and on-site monitoring, source document review and query resolution, with a focus on oncology trials and RECIST criteria. Works closely with site personnel, investigators and project teams to support study delivery.
Newcastle University Newcastle upon Tyne £30,180 pa
Support ongoing research in the Murray lab on the mechanism of DNA in bacteria, using standard microbiology techniques, bacterial two-hybrid assays, and AlphaFold3 to predict protein-protein interfaces. The post also provides direct support to a cohort of undergraduate research students, working within a professional technical community under the Biosciences Institute Technical Manager.
