Latest clinical research associate Jobs

NIS P&D Study Delivery Lead, Associate Director

The NIS P&D Study Delivery Lead, Associate Director, is responsible for leading the full lifecycle of clinical studies and trials within the Non-Interventional Study (NIS) portfolio. This includes designing, executing, and reporting complex regulatory commitment studies, managing team members, and ensuring compliance with regulatory guidelines. The role also involves leading operational decision-making, risk management, and driving innovation in study delivery through new technologies.

GSK Stevenage, United Kingdom £87,000 pa

Hybrid Permanent

NIS P&D Study Delivery Lead, Associate Director

The NIS P&D Study Delivery Lead, Associate Director, is responsible for leading the full lifecycle of clinical studies and trials within the Non-Interventional Study (NIS) portfolio. This includes designing, executing, and reporting complex regulatory commitment studies, managing team members, and ensuring compliance with regulatory guidelines. The role also involves leading operational decision-making, risk management, and driving innovation in study delivery through new technologies.

GSK £87,000 pa

Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and site selection criteria. The role also involves training and supporting site-facing colleagues, participating in safety review meetings, and contributing to continuous improvement initiatives.

Pfizer

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity 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 supporting site selection, training, and continuous improvement initiatives to enhance clinical trial execution.

Pfizer

On-site Permanent

Global Medical Affairs Director, Autoimmune Diseases

The Global Medical Affairs Director leads strategic and operational programs for autoimmune diseases, focusing on innovative evidence, launch readiness, and post-market solutions. They develop and execute medical/scientific engagement strategies, provide expert input on clinical trials, and collaborate with internal and external stakeholders to maximize the value of Novartis medicines.

Novartis London, United Kingdom

Hybrid Permanent

Global Medical Affairs Director, Autoimmune Diseases

The Global Medical Affairs Director is responsible for developing and implementing strategic and operational programs for autoimmune diseases, focusing on innovative evidence, launch readiness, and post-market solutions. They lead medical-scientific input, evidence generation, and stakeholder engagement to maximize the value of new medicines and support global medical affairs initiatives.

Novartis

Hybrid Permanent

Respiratory Account Specialist Devon & Cornwall

This role involves leading the strategy for respiratory care in hospitals across Devon and Cornwall, using data-driven insights to develop advocacy and improve patient pathways. You will partner with medical and market access teams to translate insights into actionable plans, focusing on high-value accounts and delivering measurable business impact.

AstraZeneca Exeter, United Kingdom

On-site Permanent

Respiratory Account Specialist Devon & Cornwall

This role involves leading the strategy for respiratory care in hospitals across Devon and Cornwall, using data-driven insights to develop advocacy and improve patient pathways. You will engage with NHS stakeholders, orchestrate omnichannel interactions, and focus on high-value accounts to drive measurable business impact.

AstraZeneca Plymouth, United Kingdom

On-site Permanent

Senior Director Translational Data Sciences

This role involves developing and executing a translational data strategy that bridges the gap between disease biology and clinical outcomes. The Senior Director will lead a team in integrating multi-omics data with AI-driven analytics, forming strategic partnerships, and ensuring clinical relevance in all analytical platforms.

GSK Stevenage, United Kingdom

On-site Permanent

Principal Medical Writer

This role involves authoring and delivering high-quality clinical regulatory documents, leading cross-functional teams, and managing complex writing projects. The Principal Medical Writer will interpret clinical and statistical data, ensure compliance with regulatory requirements, and contribute to global regulatory submissions.

GSK Stevenage, United Kingdom

Hybrid Permanent