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

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, collaborate with R&D and clinical development, and establish high-value partnerships with external organizations.

GSK

On-site Permanent

Principal Medical Writer

The Principal Medical Writer will author and deliver high-quality clinical regulatory documents, lead cross-functional teams in developing clinical dossier documents for global regulatory submissions, and manage complex writing projects. They will interpret complex clinical and statistical information, ensuring compliance with GSK standards and regulatory requirements.

GSK

Hybrid Permanent

Senior Regulatory Associate

The Senior Regulatory Associate at Pfizer is responsible for managing regulatory activities for assigned products and markets, including new registrations, MA variations, and renewals. They will work closely with cross-functional teams, national regulatory authorities, and above-country hubs to ensure compliance and support clinical development activities.

Pfizer United Kingdom

Hybrid Permanent

AI Acceleration Lead

This role focuses on driving AI innovation in clinical development by identifying operational bottlenecks, designing and running AI pilots, and translating findings into scalable solutions. The person will work across clinical operations, technology teams, and vendors to validate AI tools, generate evidence of value, and guide investment decisions. Emphasis is placed on hands-on testing, change management, and enterprise-wide adoption of AI-native capabilities.

GSK Stevenage, United Kingdom

On-site Permanent

AI Acceleration Lead

Lead the design and execution of AI pilots to solve operational challenges in clinical development, working across clinical operations, technology teams, and vendors. Drive evidence-based scaling of AI solutions, validate feasibility using AI-native tools, and translate findings into strategic recommendations for enterprise adoption.

GSK United States

On-site Permanent

AI Acceleration Lead

The role involves identifying and executing AI-driven pilot projects to solve operational challenges in clinical development, working closely with clinical teams, technology partners, and vendors. The focus is on validating AI solutions, measuring impact, and driving scalable adoption across GSK’s Development Operations. It emphasizes hands-on testing, evidence-based decision-making, and translating innovation into measurable improvements in trial delivery and patient outcomes.

GSK

On-site Permanent

AI Acceleration Lead

This role focuses on driving AI innovation within clinical operations at GSK, identifying high-impact use cases, designing and running AI pilots, and translating findings into scalable solutions. The position works across clinical teams, technology partners, and enterprise AI functions to validate AI tools, improve trial delivery, and deliver measurable operational value through hands-on prototyping and cross-functional collaboration.

GSK

On-site Permanent

AI Acceleration Lead

This role focuses on driving AI innovation within clinical operations at GSK by identifying high-impact opportunities, designing and running AI pilots, and translating results into scalable solutions. The AI Acceleration Lead will work across clinical, technical, and business teams to validate AI tools, measure value, and guide enterprise adoption—ensuring AI delivers measurable improvements in trial delivery and patient outcomes.

GSK

On-site Permanent

AI Acceleration Lead

The AI Acceleration Lead at GSK drives the design and execution of AI pilots to solve real operational challenges in clinical development. Working across clinical operations, technology teams, and external partners, the role focuses on testing AI solutions, validating impact, and guiding decisions on scaling. The position emphasizes hands-on use of AI tools, evidence-based evaluation, and change management to embed AI into clinical workflows and deliver measurable improvements in trial delivery and patient outcomes.

GSK

On-site Permanent