Latest Clinical Research Associate Jobs

Director, Quantitative Systems Pharmacology

This role involves leading the development and application of quantitative systems pharmacology (QSP) models to enhance drug discovery and development. Responsibilities include building mechanistic models, collaborating with cross-functional teams, and driving model-informed drug development strategies.

GSK United States

Director, Quantitative Systems Pharmacology

This role involves leading the development and application of quantitative systems pharmacology models to enhance drug discovery and development. Responsibilities include building mechanistic models, collaborating with cross-functional teams, and driving model-informed drug development strategies.

GSK

Hybrid Permanent

Central Monitor (Data Surveillance Lead)

The Central Monitor (CM) is responsible for overseeing clinical trials through centralized monitoring, ensuring data quality, identifying risks, and collaborating with cross-functional teams. Key responsibilities include executing monitoring strategies, conducting data surveillance, and supporting risk management processes.

Novartis

GCP Compliance Director (Program & Study)

Lead a team of GCP Compliance Managers to ensure global clinical trials adhere to Good Clinical Practice and regulatory standards. Drive inspection readiness, audit oversight, and quality issue management across clinical development programs. Shape compliance strategy and foster a culture of quality and continuous improvement within a matrixed pharmaceutical environment.

Novartis London, United Kingdom £83,510 – £155,090 pa

Hybrid Permanent

Field Service Engineer, Medical Diagnostic Systems

This role involves servicing, installing, repairing, and calibrating sophisticated diagnostic systems in pathology departments and NHS laboratories. You will support flow cytometry, cell separation, and diagnostics products, requiring a strong background in electronics or electro-mechanical service and excellent customer service skills.

TRS Consulting Bromley, London, United Kingdom £52,000 pa

Field Service Engineer, Medical Diagnostic Systems

This role involves servicing, installing, repairing, and calibrating sophisticated diagnostic systems in pathology departments and NHS laboratories. You will support flow cytometry, cell separation, and diagnostics products, requiring a strong background in electronics or electro-mechanical service and excellent customer service skills.

TRS Consulting Filton, Gloucestershire, United Kingdom £52,000 pa

(Fixed Term) Laboratory Technician, Clinical Biomarker Laboratory, Immunoassay

This role involves hands-on laboratory work supporting immunoassay development and clinical testing for Moderna’s mRNA-based therapeutic programs. The technician will prepare reagents, conduct sample analysis, ensure regulatory compliance, and contribute to high-quality data generation for clinical trials. Based in Oxford, the position requires full-time on-site work in a regulated lab environment with occasional overtime.

Moderna Oxford, United Kingdom

On-site Contract

Scientist, Clinical Biomarker Laboratory, Immuno-Assays - Cell Based

This role involves leading the development, qualification, and execution of complex cell-based immunoassays to support Moderna’s clinical trials across multiple therapeutic areas. The scientist will generate high-quality, reproducible data in compliance with GCP and GLP standards, while serving as a subject matter expert and collaborating with cross-functional teams. Emphasis is placed on innovation, scientific rigor, and advancing mRNA-based medicine through robust assay design and data analysis.

Moderna Oxford, United Kingdom

Hybrid Permanent

VP, Clinical Operations and Data Management

Leads the end-to-end delivery of global clinical trials from start-up to close-out, ensuring compliance, data integrity, and on-time execution. Oversees clinical operations and data management functions, including vendor and site management, database design, and regulatory coordination. Focuses on strategic planning, cross-functional collaboration, and team development within a regulatory-compliant environment.

Orchard Therapeutics London, United Kingdom

Hybrid

Global Safety Lead - Formulation Safety

Leads global safety strategy for formulation safety across the product lifecycle, focusing on clinical safety evaluation, signal detection, and risk management. Oversees production of key pharmacovigilance documents and ensures compliance with regulatory standards. Acts as safety representative in cross-functional teams and drives safety specifications and risk mitigation plans.

CSL

Global Safety Lead - Formulation Safety

Leads global safety strategy for formulation safety within CSL's GSPV department, overseeing clinical safety evaluation across product lifecycles. Responsible for signal detection, risk management planning, and regulatory compliance across clinical development and post-marketing phases. Serves as safety representative in cross-functional teams, ensuring alignment with medical, regulatory, and business objectives.

CSL

Executive Director, Asset Team Lead

The Executive Director, Asset Team Lead, will drive the strategic positioning of clinical assets in oncology and immunology, leveraging Recursion's proprietary OS and ClinTech insights. This role involves cross-functional collaboration to ensure the advancement of transformative medicines, with a focus on competitive positioning and patient benefit.

Recursion United Kingdom

Biomedical Scientist - Specialised Microbiology

This role involves performing routine and specialist microbiological and molecular investigations, interpreting and reporting results, and maintaining high professional and technical standards in a public health laboratory. The scientist will work across various laboratory sections, including Bacteriology, Serology, and Molecular Diagnostics, and contribute to quality improvement activities.

NHS Professionals Great Shelford, Cambridgeshire, United Kingdom £20 – £24 ph

Multi-Skilled Engineer II

The Multi-Skilled Engineer II role involves maintaining and repairing pharmaceutical equipment and facility installations to support manufacturing and QC operations. Responsibilities include diagnosing and repairing equipment, conducting risk assessments, planning maintenance, managing critical spares, and providing support to other teams.

Autolus Stevenage, United Kingdom

Senior Manager, PV Operations

This role leads global pharmacovigilance operations for a gene therapy company, overseeing safety case management, regulatory reporting, and compliance across clinical and post-marketing portfolios. The individual ensures robust, scalable processes and systems, including vendor oversight, safety database administration, and audit readiness. They play a key technical and operational role in SOP development, inspection preparedness, and cross-functional collaboration to support signal detection and risk management.

Orchard Therapeutics London, United Kingdom

Hybrid Permanent