Latest Clinical Research Associate Jobs

NIS P&D Project Management, Associate Director

The NIS P&D Project Management, Associate Director is responsible for developing and delivering high-quality Non-Interventional Studies (NIS) project plans, managing resources, and collaborating with various functional teams. Key responsibilities include maintaining accurate project schedules, driving cost and resource forecasts, and ensuring alignment with strategic goals.

GSK

Hybrid Permanent

ViiV Healthcare (GSK) Senior Director, Clinical Development

As a Senior Medical Director at ViiV Healthcare, you will lead the design and delivery of early development plans for HIV treatments, ensuring clinical excellence and medical governance across Phase 1-4 studies. You will collaborate with internal and external stakeholders to design, execute, and interpret clinical studies, focusing on long-acting medicines and ensuring patient safety and data integrity.

GSK United States

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and support for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves collaborating with various stakeholders, ensuring data integrity, and supporting site selection and training.

Pfizer

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and support for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves collaborating with various stakeholders, ensuring data integrity, and supporting site selection and training.

Pfizer

On-site Permanent

Director Data Science & Agentic AI

Leads the design and deployment of agentic AI systems—such as multi-agent architectures and tool-using LLMs—within Novartis' Global Drug Development to accelerate drug development timelines. Responsible for technical execution, governance, and strategic direction of AI initiatives across clinical, translational, and regulatory domains. The role involves building evaluation frameworks, ensuring regulatory compliance, mentoring AI teams, and driving innovation through research and external collaboration.

Novartis London, United Kingdom £100,240 – £186,160 pa

Hybrid Permanent

Director, Evidence Generation

This role involves leading the scientific oversight of global evidence generation studies, from Phase IIIb/IV trials to real-world evidence programmes. You will develop and implement integrated evidence strategies, influence product medical strategy, and engage with global stakeholders, including key opinion leaders and patient organisations.

Novartis London, United Kingdom

Hybrid Permanent

Senior Strategy Director (Senior Consultant) – Clinical Development – Evinova

This role involves leading the development and implementation of AI and digital health strategies to transform clinical development processes. The Senior Strategy Director will act as a trusted advisor, designing digital solutions for patient recruitment, remote monitoring, and data collection while driving innovation through AI. They will lead cross-functional teams, shape operating models, and ensure digital tools are integrated into clinical protocols with a focus on measurable value and patient outcomes.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Associate Strategy Director (Associate Consultant) - Clinical Development

This role involves shaping AI and digital health strategies to accelerate clinical development within a collaborative, innovation-driven team. You'll work across project design, protocol development, and digital solution implementation, supporting pharmaceutical partners and AstraZeneca R&D. The position emphasizes strategic consulting, technical evaluation of digital tools, and driving value through scalable, patient-centric innovations in clinical trials.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Principal Scientist, Immunogenicity and Ligand Binding Assays

This role involves leading scientific strategy and execution for immunogenicity and ligand binding assay (LBA) bioanalysis within Moderna’s mRNA-LNP therapeutic development programs. The Principal Scientist will oversee regulated assay development, validation, and sample testing, ensuring compliance with GcLP, GLP, and regulatory standards. The position emphasizes cross-functional collaboration, data interpretation, and integration of emerging technologies, including AI-enabled analytics, to support clinical decision-making across the drug development lifecycle.

Moderna

Hybrid Permanent

Senior Automation Engineer, Laboratory Automation & Biobanking

This role involves designing and optimizing automated laboratory workflows for biomarker testing and sample management within Moderna’s Clinical Biomarker Laboratory. The engineer will lead integration of advanced liquid handling systems, develop data pipelines, and ensure compliance with regulatory standards, while collaborating across digital, operations, and vendor teams to build scalable, AI-enhanced automation platforms.

Moderna

Hybrid Permanent

Director, QA Manufacturing

This role involves leading and developing the Front Line QA function at Seqirus Liverpool, ensuring pharmaceutical quality across all products. Responsibilities include providing 24/7 QA coverage, overseeing batch review and IT systems, and ensuring compliance with regulatory requirements. The role holder may also act as a QP, certifying and releasing products to market.

CSL United Kingdom

On-site Permanent

GLP/GCLP Vendor Oversight and QA Lead (EU)

This role involves leading the quality oversight of external partners in R&D and regulated activities, managing the vendor lifecycle from due diligence to continuous improvement, and ensuring compliance with GLP/GCP/GMP/GVP standards. The position requires close collaboration with various departments to maintain high-quality standards and regulatory compliance.

CSL United Kingdom

On-site Permanent