Latest clinical research associate Jobs

Associate Director, Operations Excellence Supported Studies

This role focuses on strengthening the operational and digital foundations of GSK's Supported Studies program. The Associate Director will lead data governance, system ownership, and digital integration efforts, ensuring data integrity, compliance, and efficiency across platforms like Veeva and IdeaPoint. The position acts as a bridge between business and technology, driving process improvements and digital transformation in a regulated clinical environment.

GSK US$154,275 – US$257,125 pa

Hybrid Permanent

Associate Director, Operations Excellence Supported Studies

This role leads the operational and digital foundations for Supported Studies at GSK, ensuring data integrity, system performance, and compliance across platforms like Veeva and IdeaPoint. The individual will drive process improvements, support regulatory reporting such as Transfer of Value, and act as a bridge between business and technology teams to enhance efficiency and scalability in clinical operations.

GSK US$154,275 – US$257,125 pa

Hybrid Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing, executing, and interpreting clinical studies, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally.

Pfizer

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (MD)

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing, executing, and interpreting clinical studies, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally.

Pfizer United States

On-site Permanent

Precision Medicine Director

The Precision Medicine Director leads biomarker and diagnostic strategy development for global clinical programs in neuroscience, ensuring alignment with regulatory and clinical objectives. This role involves leading cross-functional teams, designing patient selection approaches, and supporting regulatory submissions. The position operates at the intersection of clinical development, diagnostics, and precision medicine, with a strong focus on scientific rigor and compliance.

Novartis London, United Kingdom

Hybrid Permanent

Precision Medicine Director

Job Description Summary#LI-HybridWork Arrangement: Hybrid WorkingNovartis is unable to offer relocation support: please only apply if accessible.The Precision Medicine Director is responsible for developing and executing precision medicine strategies aligned to disease area and clinical program objectives. This role leads...

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

Senior Specialist, Data Science

Job Title: Senior Specialist, Data Science — Operational Data Strategy (ODS), BioPharma R&DLocation: United KingdomCompetitive Salary & Excellent Company Benefits!Introduction to the Role:The Operational Data Strategy (ODS) function provides strategic oversight for how clinical operations data is collected, organized, validated,...

AstraZeneca Cambridge, United Kingdom

VP & Global Head, Discovery Chemistry and DMPK, Oncology Targeted Delivery

This role involves leading the global Discovery Chemistry and DMPK function within AstraZeneca's Oncology Targeted Delivery (OTD) organization. Responsibilities include setting strategic direction, driving innovation in small molecules, ADCs, and RCs, and fostering a high-performing, collaborative culture across R&D sites.

AstraZeneca United States

On-site Permanent

Senior Clinical Trial Case Manager

This role involves leading cross-functional teams in reviewing safety data, mentoring junior staff, and ensuring compliance with GxP guidelines and international regulations. The position also focuses on managing pharmacovigilance procedures, conducting impact assessments of new legislation, and supporting regulatory inspections and audits.

CSL

On-site Permanent

Senior Clinical Trial Manager

Manages clinical trial operations from start-up to closure, coordinating with CROs and internal teams to ensure timely delivery of trials in oncology and rare diseases. Focuses on process improvements and operational excellence within a fast-paced, AI-driven drug discovery environment.

Recursion London, United Kingdom £62,400 – £84,000 pa

Hybrid Permanent

Senior Clinical Project Manager

The Senior Clinical Project Manager will lead the execution of one or more clinical trials from start to finish, ensuring compliance with regulations and managing cross-functional teams. This role involves planning, budgeting, and overseeing global clinical trials, with a focus on early phase oncology studies.

Recursion United Kingdom £165,900 – £211,100 pa

Hybrid Permanent

Senior Director Global Clinical Program Lead Cardiovascular & Renal

This role involves leading the clinical development of a medicine for cardiovascular and renal conditions, managing a cross-functional team, and ensuring compliance with regulatory standards. Responsibilities include strategic planning, clinical oversight, and authoring key documents for regulatory submissions and publications.

CSL Switzerland

On-site Permanent

Sales Manager (Clinical Diagnostic Services)

This role involves driving new business and expanding customer relationships in the UK health and wellness screening market within clinical diagnostics. The candidate will lead tender processes, develop commercial opportunities, and collaborate with technical teams to deliver tailored solutions. It's ideal for someone with a scientific background looking to transition into a commercial role focused on strategic growth in a science-led environment.

VRS UK Oxford, Oxfordshire, United Kingdom £50,000 – £60,000 pa

Hybrid Permanent

(Fixed Term) Data Quality Control Specialist. Clinical Biomarker Laboratory

The Data QC Specialist will perform detailed quality control reviews of laboratory data and documentation to ensure accuracy, traceability, and compliance with regulatory standards. This role involves working closely with laboratory scientists and data management teams to resolve data discrepancies and maintain inspection readiness.

Moderna Oxford, United Kingdom

On-site Temporary

(Fixed Term) Data Quality Control Specialist. Clinical Biomarker Laboratory

The Data QC Specialist will perform detailed quality control reviews of laboratory data and documentation to ensure accuracy, traceability, and compliance with regulatory standards. This role involves working closely with laboratory scientists and data management teams to resolve discrepancies and maintain inspection readiness.

Moderna

On-site Temporary