Latest Clinical Research Associate Jobs

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to the study team and external stakeholders.

Pfizer

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and collaboration with internal and external stakeholders.

Pfizer

On-site Permanent

Sr. Research Associate, Bioanalytical & Molecular Assays - Ligand Binding Assays

This role involves developing, optimizing, and validating ligand-binding and cell-based assays to support mRNA medicine development. The candidate will generate pharmacodynamic and immunogenicity data in compliance with GcLP, using platforms like Watson LIMS and electronic lab notebooks. They will also contribute to reagent management, assay documentation, and cross-functional collaboration with clinical teams to ensure robust, regulatory-compliant data delivery.

Moderna Oxford, United Kingdom

Hybrid Permanent

Sr. Research Associate, Bioanalytical & Molecular Assays - Ligand Binding Assays

This role involves developing, optimizing, and validating ligand-binding and cell-based assays to support mRNA medicine development. The candidate will generate pharmacodynamic and immunogenicity data from clinical samples in compliance with GcLP standards, using platforms like Watson LIMS and electronic lab notebooks. The position emphasizes regulatory compliance, critical reagent management, and collaboration with cross-functional teams to deliver high-quality bioanalytical data for clinical programs.

Moderna

Hybrid Permanent

Associate Director, Technology & Scientific Computing

This role involves leading the design and delivery of R-based analytics platforms and Shiny dashboards for clinical and statistical applications within a global pharmaceutical context. The individual will bridge business stakeholders, biostatisticians, and technical teams, ensuring solutions align with clinical trial workflows and regulatory standards. Key focus areas include requirement translation, end-to-end traceability, and integration of R with enterprise systems.

Novartis

Remote Permanent

(Senior) Clinical Development Medical Director

Job Description Summary#LI-HybridWork Arrangement: Hybrid WorkingLocation: London (The Westworks), United KingdomRelocation Support: This role is based in London, United Kingdom. Please only apply if accessible.Are you passionate about shaping the future of clinical development and making a meaningful impact in...

Novartis London, United Kingdom

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of clinical trials for hematological malignancies, collaborating with a multidisciplinary team to ensure patient safety, scientific integrity, and regulatory compliance. This role involves medical monitoring, data review, and strategic partnerships with thought leaders in the oncology field.

GSK United States

Hybrid Permanent

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of phase 1-3 clinical trials for hematological malignancies. This role involves collaborating with a multi-disciplinary team to ensure patient safety, scientific integrity, and regulatory compliance, while contributing to the end-to-end development of oncology drugs.

GSK

Hybrid Permanent

Associate Director, Medical Affairs

This role involves shaping and executing medical strategy for immunology products across their post-launch lifecycle, with a focus on scientific engagement, evidence generation, and collaboration with key opinion leaders and internal teams. The position supports global medical and scientific communication, contributes to clinical understanding, and aligns with commercial and research partners. Based in Maidenhead or Zurich, it operates in a hybrid model with three days onsite weekly.

CSL

Hybrid Permanent

Associate Director, Regulatory Affairs

This role involves leading the development of global regulatory strategies for drug development programs, managing regulatory activities, and collaborating with cross-functional teams. The position requires extensive experience in regulatory affairs, with a focus on global health authorities and regulatory submissions.

Recursion North Tyneside, NE29 8EP, United Kingdom

On-site Permanent

Senior Alliance Manager, London

This role involves managing and nurturing strategic scientific and business partnerships in a cutting-edge AI-driven drug discovery environment. The Senior Alliance Manager will oversee alliance governance, align internal and external teams, and ensure successful delivery of collaborative research and development programs. The position plays a key role in scaling operational frameworks and fostering a collaborative culture across high-impact partnerships.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Clinical Research Scientist

This role involves the critical review and evaluation of clinical data from scientific literature and post-market sources, supporting regulatory compliance for medical devices. The Clinical Research Scientist will prepare technical and clinical evaluation reports aligned with MDR and IVDR standards, ensuring CE marking requirements are met. Emphasis is placed on scientific writing, data analysis, and cross-functional communication within a regulated manufacturing environment.

Randstad Delivery Witney, Oxfordshire, United Kingdom £32,500 pa

On-site Contract

Clinical Data Analyst – Evinova

The Clinical Data Analyst role involves managing and optimizing clinical trial data, collaborating with cross-functional teams, and contributing to the development of data products. Responsibilities include data management, standards validation, pipeline configuration, troubleshooting, and continuous process improvement.

AstraZeneca London, United Kingdom

On-site Permanent

Clinical Project Manager

As a Clinical Project Manager, you will manage clinical trial packaging and distribution projects from start to finish, acting as the main point of contact for clients and coordinating cross-functional teams. You will ensure projects meet timelines, budgets, and quality standards while maintaining compliance with GMP/GDP requirements and client processes.

Yolk Recruitment Blackwood, Cymru / Wales, United Kingdom £45,000 pa

Hybrid Permanent

Senior Director, CGR Agentic AI Innovation

Lead the development and deployment of agentic AI systems within AstraZeneca’s Centre for Genomics Research to transform scientific workflows in genomics, multi-omics, and translational research. Translate cutting-edge AI advances into practical solutions that accelerate drug discovery and clinical decision-making by collaborating with scientists, clinicians, and engineers. Drive innovation through rapid prototyping, external partnerships, and mentorship across the R&D ecosystem.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent