Latest clinical research associate Jobs

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

Global Study Manager

The Global Study Manager role involves leading the operational delivery of clinical studies from initiation to archiving, ensuring timelines, quality, and budget adherence. Key responsibilities include crafting delivery plans, leading the Operational Working Group, and ensuring compliance with ICH/GCP guidelines. The role emphasizes innovation, risk management, and stakeholder communication.

GSK

Hybrid Permanent

Privacy Lead – R&D / Chief Patient Office (CPO)

This role involves leading privacy strategy and compliance for R&D and patient-focused initiatives at GSK, ensuring responsible data use in clinical research, digital health, and AI-driven projects. The Privacy Lead embeds privacy-by-design principles, conducts risk assessments, and supports governance across highly regulated environments, balancing innovation with ethical data practices.

GSK

Hybrid 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

Head of Medical & Scientific Affairs - Respiratory & Immunology

This role involves leading the national medical strategy for respiratory and immunology therapies within the UK NHS landscape, focusing on transforming patient care pathways and accelerating access to innovative treatments. The individual will drive pre-launch and launch readiness initiatives, shape real-world evidence generation, and collaborate with cross-functional teams and external stakeholders including NICE and MHRA. Leadership of field medical teams and strategic input into regulatory, market access, and digital health initiatives are central to the position.

AstraZeneca London, United Kingdom

Hybrid Permanent

Head of Medical & Scientific Affairs - Cardiovascular, Renal & Metabolic

Leads national medical strategy for cardiovascular, renal, and metabolic therapies, shaping policy, driving NHS collaborations, and accelerating patient access to innovative treatments. Champions real-world evidence, scientific launch readiness, and cross-functional medical execution across the UK healthcare system.

AstraZeneca London, United Kingdom

Hybrid 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 & 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

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