Latest Clinical Research Associate Jobs

Director, Digital Medicine: Respiratory, Immunology & Inflammation Research Unit

This role involves leading the development and implementation of digital medicine strategies to support clinical programs and studies in respiratory, immunology, and inflammation. The Director will guide cross-functional teams in designing digital biomarkers, endpoints, and measures, and collaborate with external partners to enhance clinical trial efficiency and patient-centric outcomes.

GSK Exeter, EX4 4HD, United Kingdom

On-site Permanent

Executive Director, External Strategy & Science Advocacy

This role involves leading the external engagement and policy advocacy for GSK's Development Sciences, working with regulatory bodies, industry consortia, and academic institutions to shape the future of pharmaceutical innovation. Key responsibilities include developing policy strategies, advancing technical capabilities, and building strategic partnerships.

GSK United States

On-site Permanent

Director, AI Engineering--Clinical Development and Operations (CD&O)

This role involves designing and deploying production-grade AI systems to enhance clinical development and operations at Pfizer. The director will lead the implementation of LLMs and agentic AI, building scalable, reproducible workflows that improve clinical trial processes such as protocol feasibility, site selection, and supply forecasting. They will collaborate closely with scientific and operational teams to translate complex needs into trusted, enterprise-scale AI solutions while championing MLOps and data governance best practices.

Pfizer United States US$176,600 – US$294,300 pa

On-site Permanent

Director, AI Engineering--Clinical Development and Operations (CD&O)

This role involves leading the design and deployment of production-grade AI systems within Pfizer's Clinical Development & Operations organization. The Director will focus on applying LLMs and agentic AI to real-world clinical workflows, building scalable MLOps pipelines, and translating complex data into decision-support tools. They will collaborate closely with scientists and digital teams to drive trusted, enterprise-wide AI adoption in a regulated environment.

Pfizer London, SW7 2AP, United Kingdom US$176,600 – US$294,300 pa

Hybrid Permanent

Medical Affairs Lead - Lung

This role involves leading the medical input for AstraZeneca's Lung Oncology portfolio, developing and delivering medical plans, and maintaining scientific relationships with key customers. The Medical Affairs Lead will also ensure regulatory compliance and support market access activities, working closely with the Therapy Area Medical Team to drive innovation and excellence.

AstraZeneca London, United Kingdom

Hybrid Permanent

Virtual Analytics Network (VAN) PhD Graduate Program

This PhD Graduate Program at Novartis involves 15 months of rotations across three key areas of the organization, focusing on clinical trials and statistical analysis. After the rotations, you will work as a Principal Biostatistician, leading statistical tasks and innovative trial designs, collaborating with multi-functional teams and external stakeholders.

Novartis Ardross, Alba / Scotland, IV17 0YF, United Kingdom

Hybrid Permanent

Trial Vendor Associate Director

The role involves managing all clinical vendor-related aspects of global clinical trials, including vendor service delivery, contract negotiations, cost control, and user-acceptance testing for eCOA and IRT systems. You will collaborate closely with the study team and ensure quality and service standards are maintained throughout the study lifecycle.

Novartis London, United Kingdom

Permanent

Regulatory Affairs Assistant

The Regulatory Affairs Assistant will provide administrative, operational, and compliance support to the Regulatory Affairs team, ensuring accurate data and documentation, supporting team processes, and maintaining compliance with regulatory standards. The role involves a broad range of activities, including regulatory file compilation, database management, project coordination, and administrative support to the Head of Regulatory and the team.

AstraZeneca London, United Kingdom

On-site Permanent

Labelling Strategy and Development, Oncology Team Lead

Lead a global team responsible for developing and managing oncology product labels, ensuring regulatory compliance and alignment with patient care and commercial goals. Drive strategic labelling governance, engage with regulatory authorities, and collaborate with cross-functional R&D teams to shape innovative, patient-focused labelling solutions.

GSK

Hybrid Permanent

Labelling Strategy and Development, Oncology Team Lead

Leads a global team responsible for developing and managing oncology product labeling strategies across the R&D lifecycle. This role ensures regulatory compliance, collaborates with cross-functional stakeholders, and shapes patient-focused labeling standards while advising senior leadership and engaging with regulatory authorities to drive innovation in labeling practices.

GSK United States

Hybrid Permanent

Labelling Strategy and Development, Oncology Team Lead

Lead a global team responsible for developing and managing oncology product labelling strategies across the R&D lifecycle. This role involves shaping compliant, patient-focused labels, advising senior stakeholders, and engaging with regulatory authorities to drive innovative approaches. The position requires strong leadership, regulatory expertise, and cross-functional collaboration within a hybrid working model.

GSK

Hybrid Permanent

Labelling Strategy and Development, Oncology Team Lead

This role involves leading a global labelling team for oncology products, shaping clear and compliant product labels that support patient care and regulatory success. The position requires strategic oversight of labelling development from early stages through lifecycle management, working closely with cross-functional teams and regulatory authorities to drive innovative, patient-focused solutions.

GSK

Hybrid Permanent

Labelling Strategy and Development, Oncology Team Lead

Leads a global team responsible for developing and managing oncology product labelling across the drug development lifecycle. This role shapes regulatory-compliant, patient-focused labels by collaborating with cross-functional stakeholders in R&D, Regulatory, Safety, and Commercial. It involves strategic decision-making, engagement with health authorities, and driving innovation in labelling standards to support GSK’s oncology portfolio.

GSK

Hybrid Permanent

Regulatory Conformance Officer (12-month / Secondment)

As a Regulatory Conformance Officer, you will ensure that GSK's products meet all licensing and regulatory requirements, maintaining compliance with global market authorisations and supporting regulatory submissions. You will collaborate with multiple functions, including manufacturing, R&D, and global regulatory affairs, to deliver regulatory strategies and inspection readiness.

GSK Barnard Castle, United Kingdom

On-site Contract

Computational Biologist

The role involves applying expertise in -omics and imaging, using state-of-the-art computational methods to support drug discovery and development, particularly in Hepatology. Responsibilities include generating and evaluating genomic and histopathology imaging evidence, collaborating with multi-disciplinary teams, and communicating results to peers and leaders.

GSK Stevenage, United Kingdom

Hybrid Permanent