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 investigators.

Pfizer

On-site 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

Global Development Lead, Early Clinical Development, Internal Medicine

The Global Development Lead will drive clinical research for cardiometabolic diseases, creating and executing early clinical development strategies. They will work closely with cross-functional teams to translate pre-clinical observations into clinical experiments, ensuring medical and scientific excellence, and managing the delivery of clinical trial data and regulatory documents.

Pfizer Cambridge, United Kingdom

On-site 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

Head, PV and Regulatory QA

TheHead of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs, and medical affairs remain compliant...

CSL

Director, Alliance Management

This role involves leading strategic partnerships with CROs, ensuring governance, performance, and relationship management. The Director will collaborate globally, drive continuous improvement, and support cross-functional teams at AstraZeneca's Cambridge Biomedical Campus.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Project Consultant

As a Project Consultant, you will manage client relationships and oversee the delivery of high-quality projects using Patient Cloud technology. Your responsibilities include managing study portfolios, leading cross-functional teams, and ensuring project milestones are met on time and within budget.

Randstad Engineering London, United Kingdom

Medical Director, Senior Patient Safety Physician

This role involves leading the clinical safety strategy for drug projects and products, ensuring the safety and risk management of AstraZeneca's pharmaceuticals. You will work on evaluating adverse events, communicating safety data, and contributing to regulatory submissions, all while collaborating with a global team of experts.

AstraZeneca Chatham, ME4 4NP, United Kingdom

Hybrid Permanent Flexible

Senior Software Engineer (Platform)

As a Senior Software Engineer at Owkin, you will design, implement, and maintain cloud-based infrastructure and services that support complex biomedical research and business intelligence. You will own critical platform components, drive technical standards, mentor junior engineers, and collaborate with cross-functional teams to enhance productivity and security.

Owkin United Kingdom

Remote Permanent

Team Lead, Platform Services

As a Team Lead, Platform Services, you will lead the development and maintenance of cloud-based infrastructure and services that support complex biomedical research and business intelligence. You will collaborate with software engineers, data scientists, and researchers to enhance productivity, improve CI/CD pipelines, and ensure data security and compliance.

Owkin United Kingdom

Remote Permanent

Clinical Evaluation Specialist - Radiology

Clinical Evaluation Specialist - Radiology/ImagingA client of mine, a consultancy working with different software and medical devices, is looking for a Clinical Evaluation Specialist with Radiology Imaging expertise.Essential experience:2+ years of patient care experienceExpertise in radiology/imaging or similarClinical research backgroundOffered:Up...

Computer Futures London, United Kingdom £75,000 – £90,000 pa

Team / Research Leader (Translational Oncology), London

This role involves leading the development and execution of comprehensive translational strategies for Isomorphic Labs' oncology pipeline. You will collaborate with interdisciplinary teams, manage a group of biologists, and ensure the successful transition of AI-designed drugs from preclinical to clinical stages.

Isomorphic Labs United Kingdom

Hybrid Permanent

Research Scientist, Immunology

This role involves designing and executing complex in vitro assays using primary human immune cells and patient-derived tissues to support drug discovery in immunology. The scientist will contribute to target validation, mechanism of action studies, and small molecule screening, leveraging advanced technologies like flow cytometry and high-content imaging. Working within cross-functional teams, they will integrate immunology expertise into both in vitro and in vivo workstreams across the therapeutic pipeline.

Recursion Crathes, Alba / Scotland, United Kingdom £52,000 – £70,400 pa

On-site Permanent