Latest clinical research associate Jobs

CMC Leader (Director)

Leads end-to-end CMC and supply chain strategy for a physical medicine from pre-clinical development through commercialisation, including process development, regulatory filings, and lifecycle planning. Works across global matrix teams to deliver robust manufacturing processes, ensure PAI readiness, and transition responsibilities to commercial operations. Focuses on complex products such as small molecules or oligonucleotides, integrating technical, regulatory, and supply considerations.

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

Associate Director (Analytical Team Leader]), Early Chemical Development, Pharmaceutical Science

This role involves leading an analytical team in early chemical development, ensuring the delivery of high-quality analytical work to support GMP manufacturing and stability. The position requires extensive experience in analytical science, a passion for team development, and the ability to drive organizational effectiveness and innovation.

AstraZeneca Macclesfield, United Kingdom

Hybrid Permanent

Specialist Biomedical Scientist- Infectious Sciences

This role involves performing and interpreting routine and specialist biomedical investigations across infectious sciences disciplines including bacteriology, virology, parasitology, mycology, and molecular diagnostics. The scientist will work autonomously within a high-volume, ISO15189-accredited laboratory, contribute to training junior staff, support on-call and weekend rotas, and engage with innovative automated systems like the Kiestra platform. Emphasis is placed on maintaining quality standards, providing clinical advice, and participating in audit and quality assurance activities.

Synlab Taunton, Somerset, TA1 1HP, United Kingdom £39,959 – £48,117 pa

On-site Permanent

Head of Translational Sciences, Drug Design, Cambridge, MA

You will lead the Translational Science strategy, identifying biomarkers and developing assays to define clinical paths and patient selection criteria. You'll ensure scientific rigor, partner with the VP of Drug Discovery to build a world-class team, and collaborate with the London team to maintain unified scientific standards. Your role involves directing in vitro and in vivo biology operations, fostering a culture of accountability, and serving as a key internal consultant for global target discovery.

Isomorphic Labs Cambridge, United Kingdom

On-site 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

Global Program Safety Team Lead - Neuroscience

This role involves leading medical safety strategy for neuroscience drug development programs at Novartis, managing global cross-functional teams, and ensuring robust benefit-risk evaluation throughout the product lifecycle. The position requires deep expertise in safety signal detection, regulatory submissions, and mentoring safety professionals, with a strong focus on clinical development and lifecycle management. Based in London or remotely, the role plays a key part in shaping global safety standards and driving patient-centric innovation.

Novartis London, United Kingdom £104,790 – £194,610 pa

Hybrid 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

Global Labelling Director, Content (Immunology)

The Global Labelling Director, Content (Immunology) will lead the development and delivery of high-quality global labelling strategies for innovative medicines. Key responsibilities include shaping labelling content, ensuring regulatory compliance, and collaborating with cross-functional teams to support successful product submissions and patient safety.

Novartis London, United Kingdom

Hybrid Permanent

Global Labelling Associate Director, Content (Established Products)

This role involves developing and maintaining global labelling strategies and core documents for pharmaceutical products. You will lead cross-functional discussions, present labelling proposals, and ensure compliance with regulatory requirements across different markets.

Novartis London, United Kingdom

Hybrid Permanent

Global Labelling Associate Director, Content (Oncology)

This role involves developing and maintaining global labelling strategies and core documents for oncology products, ensuring compliance and consistency across different markets. You will lead cross-functional discussions, present proposals to governance bodies, and mentor colleagues while staying updated on regulatory changes and competitor activities.

Novartis London, United Kingdom

Hybrid Permanent

Global Regulatory Affairs Associate Director (Cardio-Metabolic)

This role involves leading the development and submission of regulatory documents, providing strategic direction, and negotiating with health authorities to expedite approvals. The position also focuses on ensuring compliance and timely approval of new and marketed products, serving as a regulatory liaison throughout the product lifecycle.

Novartis London, United Kingdom

Hybrid Permanent

Global Labelling Director (Team Lead), Content

This role involves leading a team of labelling professionals, developing global labelling strategies, and ensuring compliance with regulatory requirements. The Director will collaborate with cross-functional partners and drive continuous improvement in labelling processes.

Novartis London, United Kingdom

Hybrid Permanent

Global Labelling Associate Director, Content

This role involves developing and maintaining global labelling strategies and core documents for pharmaceutical products. You will lead cross-functional discussions, present labelling proposals, and ensure compliance with regulatory requirements across different markets.

Novartis London, United Kingdom

Hybrid Permanent

Global Labelling Director, Content

The Global Labelling Director, Content will lead the development and delivery of high-quality global labelling strategies for innovative medicines. Key responsibilities include shaping labelling content, maintaining core documents, and collaborating with cross-functional teams to ensure regulatory compliance and successful product submissions.

Novartis London, United Kingdom

Hybrid Permanent