Latest Clinical Research Associate Jobs

Postdoctoral Research Associate in Fungal Genetics and Molecular Diagnostics

This role involves researching the emergence of a multidrug-resistant fungal pathogen, Trichophyton indotineae, at the intersection of genomics, antimicrobial resistance, and molecular diagnostics. You will work in a multidisciplinary team to develop new diagnostic tools and contribute to clinical and public health efforts in East London.

Queen Mary University of London London, United Kingdom £38 – £42 pa

Contract

Clinical Data Strategy, Manager

This role involves leading clinical data strategy planning and execution across Translational Medicine programs, with a focus on designing fit-for-purpose data collection approaches and supporting robust decision-making. The individual will develop Data Strategy Plans, guide trial teams on data oversight, and leverage internal and external data to inform trial design—particularly in Neuroscience. The position requires deep expertise in clinical assessments, data integrity, and cross-functional collaboration in a global, fast-paced environment.

Novartis London, United Kingdom £49,140 – £91,260 pa

Hybrid Permanent

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

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

Research Fellow in Optical Biomedical Instrumentation Development

Applications are invited for a Research Fellow in Optical Biomedical Instrumentation Development to join the Department of Medical Physics and Biomedical Engineering at University College London (UCL).The successful candidate will join the internationally renowned Biomedical Optics Research Laboratory (BORL) and...

UCL London, United Kingdom £46 – £54 pa

Contract

Clinical Development Senior Medical Director - Cardiovascular

Leads clinical development for vascular programmes across early and late phases, shaping study designs and clinical development plans. Works cross-functionally with translational science, regulatory, and commercial teams to advance medicines for vascular disease, with a focus on patient impact and scientific innovation. Provides medical oversight, contributes to regulatory submissions, and guides decision-making in a matrix environment.

GSK Stevenage, United Kingdom

Clinical Development Senior Medical Director - Cardiovascular

Lead clinical development for vascular programs across early and late-phase trials, designing studies and translational plans to advance medicines for cardiovascular disease. Collaborate with cross-functional teams to shape clinical strategies, ensure regulatory compliance, and drive patient-focused innovation within GSK’s R&D pipeline.

GSK

Vendor Program Head - Global Clinical Operations

The Vendor Program Head leads the vendor strategy and management for clinical development programs within a specific disease area. Key responsibilities include overseeing vendor execution, building high-performing teams, and ensuring alignment with development priorities and quality standards.

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

Associate Director, Clinical Supply Chain

This role involves leading end-to-end clinical supply chain strategy, managing complex global trials, and optimizing logistics and inventory management. You will work closely with cross-functional teams to ensure supply strategies align with trial milestones and commercial readiness.

Recursion United Kingdom

Associate Director, Clinical Supply Chain

This role involves leading the end-to-end clinical supply chain strategy for global trials, managing complex logistics, and optimizing workflows using AI. You will work closely with cross-functional teams to ensure supply strategies align with trial milestones and commercial readiness.

Recursion United Kingdom

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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

Director of Clinical Pharmacology, Cambridge, MA

Lead clinical pharmacology strategy for small molecule programs in oncology and non-oncology areas, designing and executing studies from Phase 1 through late development. Utilize AI-driven models for PK/PD prediction, dose optimization, and regulatory submissions, while managing CROs and translating preclinical data into human dosing strategies.

Isomorphic Labs Cambridge, United Kingdom

Technician in Gene and Cell Therapy, Translational Research 12-month Fixed-Term

This role involves supporting pre-clinical research through the production and characterisation of lentiviral vectors for gene therapy. The technician will perform molecular cloning, cell culture, transfection, and quality control using flow cytometry and ddPCR. The position requires meticulous documentation, protocol optimisation, and collaboration within the translational research team to advance therapeutic development.

Orchard Therapeutics London, United Kingdom

Hybrid Contract

GCP Quality Manager (12

The Quality Manager role involves providing quality oversight across clinical activities and the Quality Management System (QMS). Responsibilities include leading and supporting audits, managing quality events, and contributing to regulatory inspection readiness. The role requires significant QA experience in the pharmaceutical or clinical research sectors, strong knowledge of GCP, GCLP, and GPvP, and experience with quality management systems and regulatory inspections.

HAYS Specialist Recruitment Ox13Pa, United Kingdom

Contract

Preclinical In-Vitro Toxicology Scientist

This role involves leading in-vitro toxicology studies within a regulated preclinical environment, focusing on assay development and execution for product safety assessment. The scientist will apply advanced cell-based methods including Neutral Red, Ames, and micronucleus assays, interpret complex biological data, and support regulatory submissions. Collaboration with internal teams and external partners is key, alongside method validation and scientific reporting in a quality-assured laboratory setting.

Hudson Shribman United Kingdom £55,000 – £70,000 pa