539 jobs for “Research Scientist”
GSK Warsaw, Poland PLN 472,500 – PLN 787,500 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 working with at least two days per week on-site.
GSK Mississauga, Canada US$189,750 – US$316,250 pa
Serves as the physician within oncology clinical program teams, leading medical monitoring, safety oversight and clinical data interpretation for genitourinary studies. Partners with the Senior Scientist and cross-functional Clinical Matrix Team on protocol development, investigator and KEE engagement, and regulatory interactions. May guide other physicians on complex multi-study programmes.
Parexel London
Lead monitoring activities for assigned oncology clinical trial sites, from site activation through closeout, conducting both onsite and remote visits, source data verification and regulatory document oversight. Partner with a dedicated sponsor in an FSP model, driving enrollment, resolving protocol deviations and supporting audit readiness. Requires at least five years of oncology clinical research experience and up to 75% travel.
IQVIA London
Lead the development of country, site and patient enrollment strategies for complex global clinical trials, analysing clinical and operational data to shape feasibility and study delivery. Present recommendations to clients and senior stakeholders, with a particular focus on APAC opportunities including China. Mentors colleagues and acts as subject-matter expert for planning tools.
NanoFCM CO., LTD Stevenage £26,000 – £40,000 pa
Field-based role installing, maintaining and servicing nano-flow cytometry instruments at customer sites across the UK and Europe, plus remote phone and email troubleshooting of hardware, software and reagents. Involves preventative maintenance scheduling, service documentation, spare parts inventory and coordinating service contracts with the sales team, following training with senior technical staff.
Fortrea Maidenhead
Monitors and oversees clinical trial sites across the Midlands, handling site initiation, monitoring visits and closeouts while ensuring GCP compliance and patient safety. Also supports feasibility assessments, investigator recruitment, vendor coordination, SAE reporting and mentoring of junior team members within a global FSP team.
University of Surrey Guildford £48,337 – £70,878 pa
Develop an independent, externally funded research programme as a Principal Investigator, applying AI and data science to human, animal and environmental health data within a One Health framework. Collaborate across medicine, veterinary science, computer science and engineering, secure UKRI/NIHR/Wellcome funding, publish high-impact work, and teach AI and data science at undergraduate and postgraduate level.
Fortrea Leeds
Prepare and handle investigational medicinal products in a cGMP clean room, applying sterile technique and GMP during live first-in-human studies. Work in pairs with Technical Officers on study set-up, dose calculations, batch records and equipment checks, with the clinic and pharmacy under one roof at an MHRA-accredited Phase I unit.
Pfizer United Kingdom - Sandwich
A 12-month industrial placement within Pfizer's Global Site and Study Operations, focused on drafting and negotiating clinical trial site contracts and budgets. The undergraduate works with an experienced Site Contracting Team Lead, gaining exposure to legal terms, regulatory requirements and process improvement projects across therapeutic areas.
IQVIA Manchester
Monitors oncology clinical trial sites through selection, initiation, monitoring and close-out visits, ensuring compliance with GCP and ICH guidelines. Tracks recruitment, regulatory submissions, CRF completion and data queries, and maintains Trial Master File documentation. Works within IQVIA UK's multi-sponsor Site Management team, with travel to sites required.
Parexel London
Oversees medical coding activities across clinical studies, managing coding dictionaries such as MedDRA and WHODrug, reviewing coded data for accuracy and compliance, and preparing coding reports for medical review. Acts as subject matter expert, delivering training and partnering with Clinical Development, Pharmacovigilance and Data Management teams to drive process improvements and regulatory compliance.
UCL London £68,284 – £76,244 pa
Develops and leads an AI-driven research programme in biomolecular design and molecular interactions, spanning protein-ligand, protein-protein and protein-nucleic acid systems. Combines structural biology, biophysics, quantitative biology and machine learning, while teaching computational biology and biomolecular design at undergraduate and postgraduate level, including a new MRes in AI for Bioscience.
University of Oxford Oxford £49,119 – £58,265 pa
Lead immunological research on vaccine responses across the LEGACY studies, profiling lymph node dynamics in younger, older and immunosuppressed individuals. The role involves sophisticated wet-lab techniques including multi-parameter flow cytometry, cell culture, systems serology, ELISpot, ELISA and single-cell RNA sequencing, alongside independent project and budget management, manuscript writing and training junior staff within Prof Katrina Pollock's group.
Pfizer United Kingdom - Walton Oaks
A 12-month industrial placement within Pfizer's Global Regulatory Sciences team, supporting the development and execution of regulatory strategies across a diverse product portfolio. Day-to-day work includes compiling regulatory project documents, clinical trial applications and dossiers, responding to health authority questions, and monitoring regulatory plans and risks. Offers cross-functional exposure across the pharmaceutical product life cycle.
University of Exeter Exeter
Computational PhD project using cell-free DNA sequencing to infer placental gene activity and dissect how genetic variants linked to adverse pregnancy outcomes affect placental function. The student develops tools to map nucleosomal footprints, integrates them with single-cell RNA-seq markers and GWAS summary statistics, and may generate new plasma data.
