Latest Clinical Research Associate Jobs

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

Regulatory Affairs Specialist

This role involves maintaining technical documentation and ensuring compliance with UK and EU MDR regulations for Class I and IIa medical devices. The specialist will support regulatory submissions, post-market surveillance, and quality management system development within a regulated environment. Collaboration with the QA Manager and ongoing product lifecycle support are key aspects of the position.

Cure Talent Upper Marlbrook, Worcestershire, B61 0RT, United Kingdom £45,000 – £50,000 pa

On-site Permanent

8a Advanced Practitioner BMS - Blood Transfusion

This role involves providing expert technical and operational leadership in blood transfusion services across two NHS hospital laboratories. The Advanced Practitioner ensures regulatory compliance, leads quality and governance initiatives, oversees specialist training, and drives continuous improvement in transfusion science. The position requires deep expertise in haematology and blood sciences, with a focus on patient safety and high-quality diagnostic delivery.

Synlab Taunton, Somerset, TA1 1HP, United Kingdom £57,528 – £64,750 pa

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

Global Labelling Associate Director, Content (Oncology)

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

Novartis

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 developing core labelling documents, collaborating with cross-functional teams, and ensuring compliance with regulatory requirements. The role involves representing global labelling in governance forums and contributing to decision-making discussions.

Novartis

Hybrid Permanent