Latest Clinical Research Associate Jobs

Executive Director, External Strategy & Science Advocacy

This role involves leading the external engagement and policy advocacy for GSK's Development Sciences, working closely with regulatory agencies, industry consortia, and academic institutions to shape the future of pharmaceutical innovation. Key responsibilities include developing policy strategies, representing the organization in external forums, and advancing technical capabilities in clinical development and data science.

GSK

On-site Permanent

Clinical Sciences Project Manager

This role involves managing and refining processes for investigator-sponsored research studies, supporting the Global Collaborative Studies Group in evidence generation, and leading the Request for Proposal study process. The candidate will work cross-functionally with various teams to ensure timely and compliant delivery of studies and contribute to the mission of advancing HIV research and treatment.

GSK United Kingdom

On-site Permanent

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

This role involves designing, building, and deploying production-grade AI systems to support clinical development and operations. Key responsibilities include developing AI/ML models, automating workflows, creating decision-support tools, and collaborating with cross-disciplinary teams to ensure solutions are reliable, scalable, and adopted in day-to-day operations. The role emphasizes practical application of LLMs and agentic AI to solve real-world business problems in a regulated environment.

Pfizer United States

On-site Permanent

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

This role involves designing, building, and deploying production-grade AI systems to support clinical development and operations. You will develop and implement AI/ML models, automate manual processes, and create decision-support tools to improve operational efficiency. The role requires strong collaboration with cross-disciplinary teams and a focus on embedding MLOps best practices.

Pfizer London, SW7 2AP, United Kingdom

Hybrid Permanent

Trial Vendor Associate Director

This 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 vendor service excellence throughout the trial lifecycle.

Novartis United Kingdom

Remote Permanent

Associate Director, Regulatory Diagnostics

Designs and leads global regulatory strategies for precision diagnostics, including companion diagnostics and in vitro devices, integrated within drug development programs. Works cross-functionally to manage submissions, health authority interactions, and compliance across lifecycle stages in a collaborative, innovation-driven environment.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Regional Regulatory Intelligence Manager

This role involves leading the regional regulatory intelligence strategy, ensuring alignment with global regulatory direction and Health Authority expectations. Responsibilities include identifying and translating regulatory intelligence into actionable insights, influencing regulatory outcomes, and driving cross-functional collaboration to embed intelligence into submission content and processes.

GSK

Hybrid Permanent

Regional Regulatory Manager

The Regional Regulatory Manager leads the development and execution of regional regulatory strategies for assigned assets, ensuring alignment with global goals and regional requirements. This role involves close collaboration with global and local teams, providing regulatory expertise, anticipating risks, and driving timely submissions and approvals.

GSK United Kingdom

Hybrid Permanent

Regional Regulatory Manager

The Regional Regulatory Manager leads the development and execution of regional regulatory strategies for assigned assets, ensuring alignment with global strategies and regional requirements. This role involves close collaboration with global and local teams to deliver timely, compliant regulatory submissions and approvals, while providing regulatory expertise and market insights to support decision-making and risk management.

GSK

Hybrid Permanent

Regional Regulatory Manager

The Regional Regulatory Manager leads the development and execution of regional regulatory strategies for assigned assets, ensuring alignment with global strategies and regional requirements. This role involves close collaboration with global and local teams, providing regulatory expertise, managing submissions and approvals, and driving cross-functional alignment to deliver best-in-class regulatory outcomes.

GSK

Hybrid Permanent

Regional Regulatory Manager

The Regional Regulatory Manager leads the development and execution of regional regulatory strategies for assigned assets, ensuring alignment with global strategies and regional requirements. This role involves close collaboration with global and local teams, providing regulatory expertise, managing submissions and approvals, and driving continuous improvement and innovation.

GSK

Hybrid Permanent

Director, DP Workstream Leader – Small Molecule Parenteral (LAIs and Oligos)

This role involves leading late-stage drug product development for sterile long-acting injectables and oligonucleotides, overseeing formulation, process development, and technology transfer across clinical and commercial phases. The position acts as a strategic bridge between CMC project teams and functional execution, ensuring regulatory robustness, supply readiness, and integrated solutions through cross-functional leadership. It emphasizes scientific excellence, risk mitigation, and patient-focused innovation within a hybrid working model.

GSK United States

Hybrid Permanent

Quality Oversight and Compliance Director

The Quality Oversight and Compliance Director at Pfizer is responsible for developing and maintaining quality plans, ensuring inspection and audit readiness, and providing quality oversight of process deviations and investigations. This role involves interpreting and applying global regulations, driving compliance, and collaborating with stakeholders to identify and mitigate risks, ensuring the quality and integrity of Pfizer's medicines and vaccines.

Pfizer Sandwich, United Kingdom

On-site Permanent

Quality Oversight and Compliance Director

The Quality Oversight and Compliance Director at Pfizer will be responsible for developing and maintaining quality plans, ensuring inspection and audit readiness, and providing oversight of process deviations and investigations. This role involves interpreting and applying global regulations, driving compliance, and collaborating with stakeholders to identify and mitigate risks, ensuring the quality and integrity of Pfizer's medicines and vaccines.

Pfizer United Kingdom

On-site Permanent

Quality Oversight and Compliance Director

The Quality Oversight and Compliance Director will lead the development and maintenance of Quality Plans, ensure inspection and audit readiness, and provide quality oversight of process deviations and investigations. This role involves interpreting and applying regulatory requirements, identifying and mitigating compliance gaps, and driving continuous improvement in pan-regulatory processes and data quality.

Pfizer London, SW7 2AP, United Kingdom

On-site Permanent