Latest Clinical Research Associate Jobs

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12 Month University Industrial Placement Student: Clinical Study Administrator

This role involves coordinating and administering clinical trials within AstraZeneca’s UK-based Local Study Team, supporting end-to-end trial processes including regulatory documentation, stakeholder communication, and financial tracking. The placement student will work closely with hospital trusts, internal teams, and external vendors across therapeutic areas such as oncology and biopharma. It offers hands-on experience in clinical trial management within a structured 12-month industrial placement programme.

AstraZeneca United Kingdom £28,000 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

Research Associate III (Peptide / Protein Chemistry)

This role involves characterising peptides and proteins using analytical chemistry techniques to support drug discovery and development. The researcher will develop and optimise assays, support formulation studies, and collaborate with discovery and CMC teams. Responsibilities include data analysis, maintaining detailed records, and contributing to bioanalytical innovation in a fast-paced lab environment.

Pfizer United Kingdom

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

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

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

Director, Portfolio Development Process & Standards Lead

Lead the development and governance of processes, standards, and SOPs for CSL's global Portfolio Development function, ensuring high-quality clinical program execution. Drive cross-functional process improvement initiatives, change management, and training curriculum development. Collaborate with leadership and stakeholders across R&D to streamline decision-making and enhance operational excellence in a dynamic biotech environment.

CSL US$250,000 – US$280,000 pa

Hybrid Permanent

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

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Director, Data Scientist - Clinical AI

Lead the development and strategic implementation of AI methodologies for clinical trial design, biomarker discovery, and drug development across AstraZeneca's BioPharmaceuticals pipeline. Drive scientific innovation in collaboration with cross-functional teams, shape regulatory standards for AI in clinical evidence, and represent the company in external scientific forums. Focus on delivering reusable, enterprise-scale AI solutions grounded in rigorous data practices and translational impact.

AstraZeneca Cambridge, United Kingdom

Director, Biostatistics

Leads statistical strategy for global clinical development in inflammation, immunology, and specialty care, with responsibility for study design, analysis planning, regulatory submissions, and cross-functional collaboration. Provides scientific leadership and oversight on complex trials, drives methodological innovation, and manages external biostatistical resources. Works closely with clinical, regulatory, and data teams to ensure high-quality, compliant statistical deliverables across the drug development lifecycle.

Appcast Enterprise Surrey, United Kingdom

Director, Oncology Translational Medicine Project Manager

The Director, Oncology Translational Medicine Project Manager, will lead project management for biomarker and diagnostic strategies across GSK’s global Oncology portfolio. Responsibilities include managing external alliances, regulatory submissions, and diagnostic target profiles, ensuring high-quality data and documentation support oncology asset development and approvals.

GSK Canterbury, United Kingdom £189,750 – £316,250 pa

Director, Oncology Translational Medicine Project Manager

This role involves managing and coordinating translational research alliances and collaborations, regulatory submissions, and diagnostic target profiles for GSK's Oncology portfolio. The Director will oversee project plans, track milestones, manage risks, and ensure high-quality data packages are delivered to support oncology asset development and approvals.

GSK United States

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