499 jobs for “clinical research associate”
IQVIA
Monitors Phase 3b and Phase 4 clinical trial sites across the UK and Ireland, performing selection, initiation, monitoring and close-out visits at a pace of 6-7 visits per month. The role involves driving subject recruitment, delivering protocol training, tracking regulatory submissions and CRF data, and maintaining Trial Master File documentation in line with GCP and ICH guidelines.
IQVIA
Monitors clinical trial sites through selection, initiation, monitoring and close-out visits in line with GCP and ICH guidelines, while driving subject recruitment and tracking regulatory submissions, CRF completion and data queries. Works within a full-service, multi-sponsor site management team, training site staff and maintaining Trial Master File documentation.
Leads clinical development strategy for hepatology assets within the Respiratory, Immunology & Inflammation Research Unit, identifying next-generation liver disease targets and progressing them to proof-of-concept. Accountable for clinical development plans, study protocols, medical monitoring and safety governance, and chairs the Clinical Matrix Team. Hybrid role with at least two days per week on-site.
Leads clinical development strategy for hepatology assets within the Respiratory, Immunology & Inflammation Research Unit, from target identification through proof-of-concept studies. Accountable for clinical matrix team leadership, protocol design, medical monitoring and safety governance, and regulatory interactions across all development phases.
Thermo Fisher Scientific
Supports clinical trial delivery by coordinating site activation, maintaining (e)TMF files, tracking regulatory documents and study metrics, and handling finance tasks such as raising POs, vendor setup, invoicing and budget tracking in systems like CERPS, Ariba, Fiori and Veeva Payments. Works within a global FSP team, liaising with investigators and site staff, conducting feasibility assessments and training new personnel.
MS Office · Word · Excel +7
Moderna · 1001–5000 people · Late stage
Sole-contributor scientist role developing and executing biochemical and molecular biology assays for PK/PD analysis, spanning genomic DNA/RNA isolation, qPCR, ddPCR, RNA sequencing, MSD, ELISA and immunoblotting. Works within Moderna's Clinical Bioanalytical team at Harwell, Oxfordshire, ensuring GcLP-compliant assay qualification and validation, troubleshooting with external CRO partners, and building internal and external mRNA-based bioanalytical capability.
MSD · LIMS · eLNB +1
University of Exeter
Applies genetic clustering to severe mental illness traits to find biologically distinct risk components affecting obesity and type 2 diabetes, using GWAS data and population biobanks. Integrates single-cell multiomic datasets to map risk pathways to neuronal and glial cell types, with CRISPR-based functional work. Multidisciplinary training in statistical genetics, bioinformatics and functional genomics.
CRISPR · GWAS
University of Exeter
An interdisciplinary PhD studentship combining computational genomics at Exeter with stem-cell biology and CRISPR editing at Cambridge. The student will analyse whole-genome sequencing data from large multi-ancestry cohorts, integrate genetic signals with epigenetic maps and AI tools like AlphaGenome, and build iPSC-derived visceral and subcutaneous adipocyte models to functionally test prioritised regulatory variants.
AlphaGenome · DNANexus · Flow Cytometry +1
Ellison Institute of Technology · 501–1000 people · Non-profit
Hands-on laboratory role supporting microbiology, molecular biology, sample processing and sequencing within the Pathogen Applications Team. Involves receiving and tracking clinical samples, preparing microbial cultures, running qPCR and sequencing workflows, and maintaining QC and documentation. Suits an early-career scientist with practical lab experience in a diagnostic or high-throughput environment.
Sequencing · Oracle Cloud
Wellcome Sanger Institute
A postdoctoral research role analysing large-scale human genetic, epigenetic and proteomic datasets, including dried blood spots, birth cohorts and cell-free DNA, to uncover the genetic basis of early-life traits and develop biomarkers for pregnancy and neonatal conditions. The work spans statistical genetics, multi-omics and methods development, with scope to tailor projects to the fellow's interests.
GitHub · Snakemake · Nextflow +1
Ipsen
Ensures clinical trials comply with quality standards, SOPs and health authority regulations, partnering with site management and therapeutic area leads. Builds cluster quality plans, leads CAPA and root cause investigations, and supports audit and inspection readiness across internal and FSP teams. Also handles local regulatory intelligence and supplier quality assessments.
Quality Risk Management System
Vertex Pharmaceuticals
Leads the development and execution of international regulatory strategy across European and Rest of World markets, from first-in-human through post-marketing. Represents Global Regulatory Affairs on core development teams, manages project plans and resources, and advises senior management. Also a people manager within the International GRA leadership team, driving process improvement and regulatory policy engagement.
EMA
SPD Development Company Ltd
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.
Microsoft 365 · Outlook · Word +2
Ipsen
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.
Closed System Transfer Devices
Fortrea
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.
Outlook · Word · Excel +1
