Latest clinical research associate Jobs

Associate Director, Operations Excellence Supported Studies

This role focuses on strengthening the operational and data foundations for Supported Studies at GSK, ensuring data integrity, system performance, and compliance. The Associate Director will lead digital integration, dashboard governance, and process improvements, acting as a bridge between business and technology teams to enhance efficiency and regulatory adherence in clinical operations.

GSK United States US$154,275 – US$257,125 pa

Hybrid Permanent

Associate Director, Operations Excellence Supported Studies

This role leads operational excellence for Supported Studies at GSK, focusing on data integrity, system governance, and digital transformation. The individual will own the data and dashboard ecosystem, act as Business System Owner for key platforms like IdeaPoint and Veeva, and ensure compliance with regulatory requirements such as Transfer of Value. They will bridge business and technology to drive process improvements, enable resource planning, and enhance data transparency across clinical operations.

GSK £154,275 – £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 and executing clinical trials, creating development plans, and ensuring regulatory compliance. The role also includes collaborating with cross-functional teams, providing expert input on clinical data, and engaging with external stakeholders to drive strategic insights.

Pfizer

On-site 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 and executing clinical trials, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally. The role also includes providing expert input on trial design, regulatory activities, and engaging with external stakeholders to drive strategic insights.

Pfizer

On-site Permanent

Trial Vendor Senior Manager - Global Clinical Operations

This role involves end-to-end management of clinical trial vendors, ensuring timely and compliant delivery of services such as eCOA, central labs, and IRT. The Senior Manager leads vendor performance, financial oversight, and system validation activities while collaborating across global teams to support trial execution. Focus areas include risk mitigation, site activation, and adherence to GxP and ICH standards within a hybrid working model.

Novartis London, United Kingdom £49,140 – £91,260 pa

Hybrid Permanent

Trial Master File Oversight Manager

This role involves overseeing the quality and completeness of Trial Master Files across global clinical trials, ensuring compliance and readiness for audits. The manager will lead vendor oversight, identify documentation risks, and drive process improvements while acting as a subject matter expert. Collaboration with cross-functional teams is essential to maintain high standards in clinical documentation and support continuous innovation in TMF systems.

Novartis London, United Kingdom £49,140 – £91,260 pa

Hybrid Permanent

Field Service Engineer, Laboratory Automation Systems

This role involves installing, servicing, repairing, and calibrating advanced laboratory automation and diagnostics systems in NHS and clinical settings. The engineer will work on complex electro-mechanical systems, including flow cytometry and cell separation equipment, providing technical support directly at customer sites. The position requires strong field service skills and the ability to operate confidently in high-pressure, customer-facing healthcare environments.

TRS Consulting Wandsworth, London, SW18 1UJ, United Kingdom £52,000 pa

On-site Permanent

Executive Director, Strategy, Oncology R&D

This role involves crafting and driving the global Oncology R&D strategy, integrating clinical, scientific, and commercial insights to shape portfolio priorities. You will advise senior leadership on complex strategic decisions, optimize investment, and collaborate across functions to deliver impactful patient outcomes.

AstraZeneca Canterbury, United Kingdom

On-site Permanent

Executive Director, Strategy, Oncology R&D

This role involves owning and driving the global Oncology R&D strategy, setting priorities for the senior executive team, and transforming the approach to deliver impact for patients. The Executive Director will lead the creation of comprehensive therapeutic area strategies, provide strategic recommendations to senior leadership, and collaborate across functions to drive innovation and impact.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Senior Security Engineer, London

As a Senior Security Engineer, you will play a crucial role in architecting and managing the security of Isomorphic Labs' AI-based platform and HPC infrastructure. You will work closely with DevOps, SRE, and other teams to ensure robust security practices, from secure architecture and IaC to threat modeling and incident response.

Isomorphic Labs United Kingdom

Hybrid Permanent

Clinical Program Manager, Cambridge, MA

The Clinical Program Manager will lead the transition of internal drug programs from pre-IND stages into clinical trial execution, coordinating cross-functional global teams and external vendors. This role involves managing timelines, budgets, risks, and stakeholder communication, while leveraging AI-driven insights to accelerate development. The position emphasizes integrated project planning and operational leadership to ensure efficient, high-probability clinical advancement.

Isomorphic Labs Cambridge, United Kingdom

Hybrid Permanent

Clinical Safety Scientist

This role involves monitoring and evaluating the safety profiles of medicines, with a focus on HIV treatments and prevention. The Clinical Safety Scientist will conduct signal detection, assess safety data, contribute to risk management plans, and support regulatory documentation across the product lifecycle. Collaboration with safety physicians and adherence to global regulatory standards are key aspects of the position.

Carbon 60 London, United Kingdom £350 – £500 pd

Hybrid Temporary

Clinical & Validation Principal

Lead bioanalytical method development and validation activities within a GxP-regulated laboratory, overseeing HPLC, UPLC, and LC-MS/MS platforms. Manage a technical team, ensure regulatory compliance, and support audits and submissions. Focus on method optimisation, troubleshooting, and continuous improvement in a highly controlled environment.

Next Phase Recruitment Armagh, County Armagh, United Kingdom

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