Latest Clinical Research Associate Jobs

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 approvals and global market access. The role also includes specialized monitoring, regulatory submissions, and engaging with external stakeholders to drive strategic insights.

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, working closely with cross-functional teams to design, execute, and interpret clinical studies. Key responsibilities include creating clinical development plans, regulatory submissions, and providing expert input on trial design and execution, while ensuring compliance and strategic insight generation.

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

GCP Compliance Manager (GCO)

This role involves leading quality issue management, audit coordination, and inspection readiness for global clinical trials, ensuring compliance with GCP and regulatory standards. The manager will drive self-assessments, conduct risk-based investigations, and provide expert guidance across clinical operations. It’s a high-impact compliance position requiring strong cross-functional influence and operational rigor in a hybrid working environment.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Senior Scientific Writer II

The Senior Scientific Writer II role involves developing high-quality medical and scientific communications for Novartis, including slide decks, congress materials, and advisory board content. The position requires strong collaboration with cross-functional teams to ensure content accuracy, consistency, and compliance with internal and external standards.

Novartis London, United Kingdom

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

Scientist, Clinical Biomarker Laboratory, Immuno-Assays - Cell Based

This role involves leading the development, qualification, and validation of cell-based immunoassays to support Moderna’s clinical trials across multiple therapeutic areas. The scientist will generate high-quality, GLP/GCP-compliant data from clinical samples, contribute to regulatory documentation, and collaborate with cross-functional teams and external partners. Emphasis is placed on scientific rigor, innovation in assay design, and mentoring junior staff within a regulated, collaborative laboratory environment.

Moderna Oxford, United Kingdom

Hybrid Permanent

(Fixed Term) Laboratory Technician, Clinical Biomarker Laboratory, Immunoassay

The Laboratory Technician will support the Immunoassay group by executing experimental work, maintaining the lab, and ensuring high-quality data for clinical trials. The role involves hands-on lab work, preparing reagents, conducting assays, and maintaining compliance with safety and regulatory guidelines.

Moderna

On-site Contract

Vice President, Head of Clinical Operations

This role involves leading the clinical operations strategy and execution across Recursion’s development portfolio, from study planning to study closeout. You will build and mentor a high-performing team, manage global trials, and ensure operational excellence in an AI-native TechBio company.

Recursion United Kingdom

On-site Permanent

Pharmaceutical Regulatory Affairs Officer

This role involves managing regulatory submissions and product lifecycle compliance for pharmaceutical products, with a focus on packaging, labelling, and interactions with the MHRA. The candidate will coordinate eCTD submissions, support variations, and ensure change control processes are followed across cross-functional teams. It's a hands-on position offering impact in a regulated environment with hybrid working and a clear regulatory focus.

Evolve Selection Leicester, Leicestershire, United Kingdom £40,000 – £50,000 pa

Hybrid

Director Biostatistics

The Director of Biostatistics leads the statistical aspects of clinical development programs, ensuring robust study design, data analysis, and regulatory submissions. They collaborate closely with cross-functional teams and regulatory authorities to drive the success of clinical trials and therapeutic programs.

CSL

Hybrid Permanent

Director Biostatistics

The Director of Biostatistics leads the statistical aspects of clinical development programs, ensuring robust data analysis and regulatory compliance. They collaborate with cross-functional teams, manage external partners, and represent Biostatistics in regulatory interactions.

CSL

Hybrid Permanent

Technical Program Manager, ClinTech Strategy & Analytics

This role involves project managing and tracking the ClinTech roadmap, working closely with Clinical Development Operations and Decision Science to translate priorities into actionable plans. You will also support the communication of ClinTech’s progress to senior leadership and external audiences, contributing to vendor assessments and build-vs-buy evaluations. The role is at the heart of a high-visibility team building a platform to accelerate drug development.

Recursion North Tyneside, NE29 8EP, United Kingdom £136,200 – £211,100 pa

Hybrid Permanent