Latest Clinical Research Associate Jobs

Global Clinical Operations AI Program Associate Director

This role leads the execution and delivery of AI initiatives within Global Clinical Operations, translating innovative concepts into scalable, compliant solutions. The Associate Director will coordinate cross-functional teams, manage the AI product roadmap, and drive adoption of AI tools across clinical trial operations. It involves strong program management, change leadership, and collaboration with technology and clinical stakeholders to transform how AI enhances productivity and compliance in drug development.

Novartis London, United Kingdom £83,930 – £155,870 pa

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 - Vascular

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 - Vascular

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

Global Development Lead, Internal Medicine, Sr. Director (MD)

Leads clinical development for assigned assets in Internal Medicine, serving as the primary clinical accountability point within Pfizer's Research & Development. Designs and oversees global clinical trials, regulatory submissions, and cross-functional team coordination, with potential involvement in obesity-related late-stage programs. Engages with external stakeholders and ensures compliance with scientific, regulatory, and safety standards.

Pfizer England

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with a focus on obesity-related therapies. The Global Development Lead will design and oversee global clinical trials, create development plans, and ensure regulatory compliance across regions including China and Japan. The position requires cross-functional leadership, engagement with external stakeholders, and contribution to regulatory submissions and product labeling.

Pfizer England £214,900 – £358,100 pa

On-site Permanent

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

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

Postdoctoral Scientist: Cancer Evolutionary Genomics

This role involves analyzing large-scale genomic datasets from kidney cancer patients across the TRACERx Renal 300 and PEACE studies, focusing on understanding cancer evolution through computational and biological approaches. The postdoctoral scientist will work with multi-sample genomic data to reconstruct clonal and phylogenetic trajectories, leveraging both primary and postmortem samples. Based in Manchester with links to the Francis Crick Institute, the position offers integration into a multidisciplinary team engaged in cutting-edge cancer genomics and translational research.

The University of Manchester Manchester, Northern England, United Kingdom £39 – £47 pa

Contract