Latest Clinical Research Associate Jobs

Spotlight

Scientist I – Molecular Biology

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.

Alloy Therapeutics UK Ltd Cambridge £45,000 – £50,000 pa

On-site Permanent

Spotlight

Senior Computational Chemist, LNP Design

This role involves leading the computational design of lipid nanoparticles for nucleic acid delivery, using chemical and biophysical principles, AI tools, and molecular simulations. You will work closely with the experimental team to translate computational insights into testable strategies and refine formulations iteratively.

CureAge Therapeutics London

Hybrid Permanent Part-time

Clinical Research Associate

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.

MSD London

Remote Permanent

Clinical Research Associate (Multiple Roles)

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.

Novartis Field Force (England / Wales) £32,690 – £60,710 pa

Hybrid

Clinical Research Associate II/ Senior Clinical Research Associate Yorkshire

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.

Fortrea Leeds

Hybrid Permanent

Clinical Research Associate, South West England

Monitors clinical trial sites across South West England, performing selection, initiation, monitoring and close-out visits in line with GCP and ICH guidelines. Tracks recruitment, regulatory submissions and data query resolution, and maintains Trial Master File documentation. Works within a sponsor-dedicated team, requiring independent on-site monitoring experience.

IQVIA Bath

Clinical Research Associate II or Senior Clinical Research Associate

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.

Parexel Harrow

Remote

Clinical Research Associate I

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.

Fortrea Maidenhead

Hybrid Permanent

Senior Clinical Research Associate

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

Senior Clinical Research Associate (Oncology Experience Required) - UK - FSP

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.

Parexel London

Remote

Sr/CRA I/II - UK (numerous locations)

Monitors investigator sites using a risk-based approach, conducting remote and on-site visits to assess protocol and regulatory compliance, performing SDR, SDV and CRF review, and documenting findings in reports. Acts as a site processes specialist ensuring trials follow ICH-GCP, applicable regulations and SOPs, while developing collaborative relationships with investigational sites and supporting audit readiness.

Thermo Fisher Scientific United Kingdom

Remote

Assistant CRA

Supports clinical trial site management remotely, liaising with CRAs and study teams on site preparedness, document collection, vendor trackers and remote monitoring tasks. Handles essential documents, site payments, reconciliations and centralized monitoring reviews in line with SOPs and ICH GCP. Suits an early-career life sciences graduate seeking a UK-based remote clinical research role.

Thermo Fisher Scientific United Kingdom

Remote

Senior Research Associate, Bioanalytical & Molecular Assays

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 contributing to SOPs, critical reagents and digital/automation improvements.

Moderna Clinical Development

Hybrid Permanent

Senior Research Associate, Bioanalytical & Molecular Assays

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

Hybrid

Bioinformatics Research Associate

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.

Imperial College London London £50,733 – £59,484 pa

Hybrid Contract

Research Associate in Human Physiology Immunology and Long COVID

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.

Loughborough University Loughborough

Hybrid Contract

Associate Director, Global Clinical Science - Neuroscience

Leads and executes clinical trial activities as Clinical Trial Lead, providing scientific and clinical leadership to a matrix team of Clinical Scientists. Involves protocol and ICF development, clinical data review and trend identification, CSR and regulatory document drafting, and serving as primary liaison with external partners. Requires strong GCP/ICH knowledge and may involve domestic and international travel.

Bristol Myers Squibb Uxbridge