Latest Clinical Research Associate Jobs

Global Program Safety Team Lead

This role involves leading the Medical Safety organization for Novartis' Neuroscience division, managing safety strategies, and influencing high-stakes decisions. Responsibilities include managing disease areas, enhancing team expertise, and ensuring robust safety evaluations throughout the product lifecycle.

Novartis United Kingdom

Hybrid Permanent

Head of Global Regulatory Affairs and Strategy, Cambridge, MA

This senior leadership role involves defining and optimizing global regulatory strategies for drug development programs, building a regulatory team and systems, and implementing quality, pharmacovigilance, and medical writing frameworks. The role leverages AI to streamline regulatory workflows and ensure rapid global approval of products.

Isomorphic Labs Cambridge, United Kingdom

On-site Permanent

Senior Safety Scientist / Associate Director / Director

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive...

Roche Welwyn Hatfield, United Kingdom

Chemical Process Operator

This role involves operating chemical process plant and manufacturing equipment, following batch manufacturing instructions, monitoring chemical reactions, and supporting material handling and packaging activities. The position offers long-term stability and development opportunities within a safety and quality-driven manufacturing environment.

Talent STEM Ltd Stradishall, United Kingdom

On-site Permanent Shift-work

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 aligning regional regulatory approaches with global objectives and managing Health Authority interactions.

Novartis

Hybrid Permanent

Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism)

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

Novartis London, United Kingdom

Hybrid Permanent

PKPD Modelling Lead, London

Isomorphic Labs is applying frontier AI to help unlock deeper scientific insights, faster breakthroughs, and life-changing medicines with an ambition to solve all disease.The future is coming. A future enabled and enriched by the incredible power of machine learning. A...

Isomorphic Labs London, United Kingdom

Safety Process Director / Senior Safety Process Director

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive...

Roche Welwyn Hatfield, United Kingdom

Trial Vendor Senior Manager

This role involves managing all vendor-related aspects of global clinical trials, ensuring study outcomes are delivered within schedule, budget, and quality standards. The Senior Manager will collaborate with the Vendor Start-up Manager and other team members, oversee vendor interfaces, and manage risks and performance.

Novartis London, United Kingdom

Hybrid Permanent

Trial Vendor Senior Manager

This role involves managing all vendor-related aspects of global clinical trials, ensuring study outcomes are delivered within schedule, budget, and quality standards. The Senior Manager will collaborate with the Vendor Start-up Manager and other team members, oversee vendor service delivery, and manage risks and performance.

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

Hybrid Permanent

Vendor Start-Up Manager - eCOA & Translations

The Vendor Start-Up Manager for eCOA and Translations ensures vendors are aligned and ready to deliver high-quality services from protocol finalization to database go-live. Key responsibilities include reviewing vendor specifications, coordinating kick-off meetings, performing User Acceptance Testing, and optimizing the study start-up process.

Novartis London, United Kingdom

Hybrid Permanent

Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism)

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

Novartis

Hybrid Permanent

Principal Statistical Programmer

The Principal Statistical Programmer leads statistical programming activities for large or pivotal clinical studies, ensuring high-quality and timely deliverables. They collaborate with cross-functional teams, mentor other programmers, and maintain compliance with industry standards.

Novartis London, United Kingdom

On-site Permanent

Assoc Director, Statistical Programming

The Associate Director, Statistical Programming, leads all statistical programming aspects for one or more drug development programs, ensuring cross-functional collaboration, resource allocation, and regulatory compliance. They coordinate activities, mentor programmers, and represent the team in audits and Health Authority meetings.

Novartis London, United Kingdom

Hybrid Permanent

Vendor Start-Up Manager - eCOA & Translations

The Vendor Start-Up Manager for eCOA and Translations ensures vendors are aligned and ready to deliver, protecting study timelines, quality, and patient experience. Key responsibilities include technical expertise, risk assessment, continuous improvement, and vendor oversight.

Novartis

Hybrid Permanent