510 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.
Pfizer · 10000+ people · Public
Accountable for planning and executing multiple complex global clinical studies, driving timelines, budgets and quality targets while leading cross-functional study teams. Provides clinical operations input into study design, oversees CRO vendors, risk management and inspection readiness, and may support program-level and submission deliverables.
Clinical Research Organization
Leads clinical development strategy for hepatology assets within the Respiratory, Immunology & Inflammation Research Unit, overseeing study design, medical monitoring, and regulatory interactions. Accountable for the Clinical Matrix Team, target validation, translational plans, and Go/No Go decision criteria across early-phase programs. Hybrid role requiring on-site presence at least two days per week.
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.
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
Johnson & Johnson Innovative Medicine
Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare analyses and evaluations for regulatory compliance. Supports Safety Management Teams, conducts proactive safety data reviews, and serves as product point of contact, with hybrid working requiring three days on site.
Microsoft Word · Microsoft Excel · Microsoft PowerPoint
Relation Therapeutics
Lead the team behind hybrid on-prem and cloud compute infrastructure, Kubernetes clusters, and scientific compute environments supporting ML and drug discovery. Own platform strategy, CI/CD maturity, observability, and security controls for sensitive patient-derived data, reporting to the VP of Engineering.
Kubernetes · Kubeflow · GPU Compute +3
University of 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.
scRNA-seq · cfDNA Sequencing · GWAS
Moderna · 1001–5000 people · Late stage
Leads the creation, review and oversight of investigator site budgets and grants across Phase I–IV clinical trials, using Grants Manager/GrantPlan and FMV benchmarking. Manages CRO site budget and CTA negotiations, scenario planning and site activation timelines, with exposure to Generative AI tools for analytics.
Grants Manager · GrantPlan · MS Office +1
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
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
NHS Professionals · 1001–5000 people · Public
Perform biochemical analyses on patient samples using manual and automated techniques, maintain and QC point-of-care testing equipment, and authorise results for electronic reporting to wards. The role includes out-of-hours rota cover, giving technical advice to clinical staff, and supporting quality management and service development in a hospital biochemistry lab.
POCT
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
