526 jobs for “Clinical Research Associate”
Alloy Therapeutics UK Ltd Cambridge £45,000 – £50,000 pa
Design and build large-scale synthetic gene loci and transgenic platforms for antibody discovery, using CRISPR/Cas9, RMCE and site-specific integrases. Hands-on molecular biology including PCR, NGS, plasmid construction and flow-cytometric immunophenotyping, within a small multidisciplinary team working from dry-lab design to wet-lab validation.
CureAge Therapeutics London
Lead the computationally guided design of a lipid nanoparticle delivery platform, applying chemical and biophysical principles to optimise LNP composition and formulation. Use AI-enabled chemistry, cheminformatics, predictive models and molecular modelling to prioritise formulation components, working closely with the experimental team and founding team in a small start-up.
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.
Novartis Field Force (England / Wales) £32,690 – £60,710 pa
Site-facing role managing Phase I–IV clinical trial sites, acting as the primary contact between the sponsor and sites. Responsibilities include site initiation visits, training, on-site and remote monitoring, risk assessment and mitigation, and closeout activities, working closely with cross-functional teams to ensure data integrity and compliance.
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.
Parexel Harrow
Monitors clinical trial sites across the UK as the sole point of contact, conducting qualification, initiation, monitoring and termination visits and producing visit reports. Manages site quality, regulatory documentation and drug accountability while developing recruitment strategies to meet enrolment timelines. Fully decentralised role with less travel and a lower protocol load than industry peers.
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.
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.
IQVIA Reading
Monitors clinical trial sites across 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 a sponsor-dedicated team, liaising with sites and study team members.
Thermo Fisher Scientific United Kingdom
Independently manages basic project tasks including budgets, timelines and client correspondence, while supporting protocol and report development under senior supervision. Conducts qualitative data collection such as cognitive interviews and focus groups, performs literature reviews and data analysis, and assists with scientific publications. Requires 10-30% travel and works within a multidisciplinary patient-centered research team.
Thermo Fisher Scientific United Kingdom
Supports patient-centered research projects by conducting literature reviews, cognitive interviews and focus groups, managing data collection and coding, and assisting with analysis and reporting. Works within a multidisciplinary team spanning psychometrics, epidemiology and health sciences, with some independent project task management.
Moderna Oxford
Perform bioanalytical assays using molecular and cellular techniques such as ddPCR, qPCR, RT-qPCR and gel electrophoresis to quantify RNA in biological matrices. Support phase-appropriate assay development, qualification and validation within a GCLP-compliant clinical framework, partnering with internal and external labs and cross-functional teams. The role blends basic science research, bioanalysis and clinical development, with exposure to digital and automation tools.
Moderna Oxford
Develops, validates and runs ligand-binding and cell-based bioanalytical assays generating pharmacodynamic and immunogenicity data for clinical mRNA programmes. Works in a GcLP-regulated lab using Thermo Watson LIMS and electronic notebooks, handling clinical samples, critical reagents, SOPs and validation reports while partnering with Clinical Operations and Sample Management.
Imperial College London London £50,733 – £59,484 pa
Lead the harmonisation, integration and analysis of large-scale multi-omics datasets including single-cell transcriptomics, epigenomics and proteomics, building reproducible Nextflow or Snakemake pipelines on HPC or cloud infrastructure. Work with AI and mathematical modelling teams within a multidisciplinary consortium spanning Imperial, UCL and industry partners on an ARIA-funded programme studying innate immune protection against respiratory viral infections.
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.
Pfizer Collegeville, United States US$176,600 – US$294,300 pa
Accountable for planning and executing multiple complex global clinical studies, driving timelines, budgets and quality from start-up through database release and inspection readiness. Leads cross-functional study teams, manages CRO vendor oversight, risk and governance milestones, and may support program-level and submission activities.
