Latest Clinical Research Associate Jobs

Spotlight

Senior Clinical Trial Case Manager

This role involves leading safety data review and pharmacovigilance activities within clinical trials, ensuring compliance with international regulations such as GxP. The individual will mentor team members, manage CAPAs, support regulatory inspections, and contribute to safety reporting and risk management. Key responsibilities include MedDRA coding, safety data analysis, and developing pharmacovigilance procedures to support global regulatory requirements.

CSL

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, ENG, United Kingdom

Hybrid Permanent Part-time

Clinical Research Associate (Multiple Roles)

This role involves managing clinical trial sites across Phase I–IV studies, ensuring protocol compliance, data integrity, and patient safety. The Clinical Research Associate conducts site visits, delivers training, monitors performance, and drives risk mitigation in collaboration with cross-functional teams. It is a field-based, site-facing position requiring strong regulatory knowledge and relationship-building skills.

Novartis United Kingdom £32,690 – £60,710 pa

Senior Research Associate, Bioanalytical & Molecular Assays

This role involves developing, qualifying, and validating molecular bioanalytical assays—such as qPCR, ddPCR, and RT-qPCR—to support clinical pharmacokinetic and pharmacodynamic studies within a GCLp-compliant environment. The scientist will work closely with cross-functional teams to ensure robust data generation, maintain regulatory compliance, and integrate emerging digital and automation technologies into workflows. A strong focus on reagent management, assay documentation, and continuous process improvement is central to the position.

Moderna Oxford, United Kingdom

Hybrid Permanent

Senior Research Associate, Bioanalytical & Molecular Assays

This role involves developing, optimizing, and validating molecular bioanalytical assays—such as qPCR, ddPCR, and RNA isolation—to support mRNA-based clinical programs. The scientist will work within GCL0-compliant (GCLP) frameworks to generate pharmacokinetic and pharmacodynamic data, ensuring regulatory compliance and data integrity. Collaboration with cross-functional teams and adoption of digital tools and automation are key to advancing clinical trial execution and analytical processes.

Moderna

Hybrid Permanent

Bioinformatics Research Associate

This role involves leading the integration and analysis of large-scale multi-omics datasets, developing computational pipelines, and collaborating with AI and mathematical modelling teams to support therapeutic discovery. You will work closely with a multidisciplinary team across academic and industry partners to deliver key project milestones and present findings at scientific conferences.

Imperial College London London, Hybrid, London, United Kingdom £50 – £59 pa

Contract

Research Associate - Proteomics

This postdoctoral position involves leading the preparation and analysis of skeletal muscle samples for proteomic and transcriptomic workflows, focusing on the 'dark proteome' in facioscapulohumeral muscular dystrophy (FSHD). The role combines technical leadership with broader involvement in translational research, collaborating with international partners.

Newcastle University Newcastle upon Tyne, Northern England, United Kingdom £36 – £46 pa

Contract

Research Associate in Human Physiology Immunology and Long COVID

The role involves conducting research on the biological mechanisms of fatigue and post-exertional symptom exacerbation in Long COVID. Responsibilities include participant recruitment, physiological assessments, biological sample collection, and project coordination, working closely with multidisciplinary teams.

Loughborough University Loughborough University, Loughborough, Hybrid/on-Site, Midlands Of England, United Kingdom £35 pa

Contract

Associate Director, Biostatistics

This role leads the statistical strategy for clinical development programs, overseeing study design, data analysis, and regulatory submissions. The individual will guide biostatistical input across trials, interact with regulatory authorities, and ensure accurate reporting of results. Collaboration with cross-functional teams and oversight of internal or outsourced programming efforts are key aspects of the position.

CSL

Hybrid Permanent

Records Management Associate

This role involves managing the security, storage, and retrieval of proprietary and client information, using scanning equipment and maintaining accurate records. The position also includes developing and implementing a sustainability strategy for IQVIA Laboratories and providing reference services to internal clients.

IQVIA Livingston, Alba / Scotland, EH54 6GS, United Kingdom

On-site Permanent

Associate Director, Biostatistics

The Associate Director, Biostatistics, leads statistical contributions to clinical development programs, including study design, data analysis, and regulatory submissions. They collaborate with cross-functional teams, manage outsourcing, and ensure the quality and timeliness of deliverables.

CSL £212,000 – £251,000 pa

Hybrid Permanent

Senior Medical Director, Oncology Clinical Development - GU

This role involves leading clinical development activities for GSK’s oncology portfolio, with a focus on genitourinary (GU) cancers. The Senior Medical Director will design and execute Phase 1-3 clinical trials, provide medical oversight, interpret clinical data, and engage with external experts and regulatory authorities. The position requires strong leadership in a matrixed environment and deep expertise in oncology drug development.

GSK Stevenage, United Kingdom US$284,250 – US$473,750 pa

Hybrid Permanent

Senior Medical Director, Oncology Clinical Development - GU

Leads clinical development for oncology assets, focusing on genitourinary (GU) cancers. Responsible for designing and executing phase 1-3 trials, ensuring scientific integrity, regulatory compliance, and collaboration with internal and external experts. Works within a global matrix to advance GSK’s innovative oncology pipeline from development through market launch.

GSK US$284,250 – US$473,750 pa

Hybrid Permanent

Research Scientist - T Cell immunology

This role involves designing and executing experimental research in T cell immunology, focusing on the immunological and functional characteristics of T cell subsets and receptors. The work includes immunophenotyping patient samples, functional assays, and molecular biology techniques, with opportunities to develop independent research projects.

University of Oxford Oxford, South East England, United Kingdom £39 – £47 pa

On-site Contract

Associate Director / Director, Biostatistics

This role involves providing strategic statistical leadership for Health Technology Assessment, pricing, and reimbursement activities. The candidate will work with cross-functional teams to ensure HTA evidence is scientifically rigorous and aligned with payer requirements. Responsibilities include implementing HTA methods, contributing to evidence synthesis, and mentoring biostatisticians.

Novartis London, United Kingdom

Associate Director, Operational Intelligence

This role focuses on building advanced operational models and simulations to optimise Autolus' end-to-end processes across manufacturing, testing, supply chain, and quality. The individual will integrate data from multiple systems to create analytical frameworks that drive strategic decisions, improve capacity planning, and support business cases. It is a highly technical, insight-driven position requiring deep expertise in data modelling, cross-functional collaboration, and problem-solving in a regulated biopharmaceutical environment.

Autolus Stevenage, United Kingdom

On-site Permanent

Scientist - Applications Team (Pathogen)

This role involves hands-on laboratory work supporting the Pathogen Applications Team at EIT. Responsibilities include sample processing, microbiology and molecular biology workflows, qPCR, and sequencing. The position is ideal for an early-career scientist with practical lab experience looking to expand their skills in a fast-paced R&D environment.

Ellison Institute of Technology Oxford, United Kingdom

On-site Permanent