Latest Clinical Research Associate Jobs

Director, Translational Science Lead

This role leads translational science strategy across renal, inflammation, fibrosis, and neurodegeneration disease areas, driving biomarker development and validation to support clinical decision-making from preclinical through to launch. The position integrates cutting-edge technologies like spatial transcriptomics and human multi-omics data, working across discovery and development to de-risk clinical transitions and identify responder populations.

GSK Stevenage, United Kingdom US$178,200 – US$297,000 pa

Hybrid Permanent

Director, Translational Science Lead

Leads translational science strategy for renal, inflammation, fibrosis, and neurodegeneration programs, driving biomarker development and validation from preclinical to clinical stages. Focuses on integrating multi-omics data, human assays, and novel technologies to inform clinical decision-making and patient stratification. Works across discovery and development to advance differentiated therapeutics through cross-functional collaboration and external partnerships.

GSK Canterbury, United Kingdom £178,200 – £297,000 pa

Hybrid 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 collaborating with various stakeholders, including external committees and site-facing colleagues, to ensure the successful execution of clinical studies.

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, protocol training, and continuous improvement initiatives to enhance clinical trial execution.

Pfizer

On-site Permanent

Global Labelling Manager, Content

The Global Labelling Manager, Content will lead the development and maintenance of high-quality global labelling documents for pharmaceutical products. Key responsibilities include organising cross-functional discussions, conducting research on competitor labels and regulatory guidance, and ensuring compliance with global standards across the product lifecycle.

Novartis London, United Kingdom

Hybrid Permanent

Global Labelling Manager, Content (Neuroscience)

The Global Labelling Manager, Content will lead the development and maintenance of high-quality global labelling documents for pharmaceutical products. Key responsibilities include organising cross-functional discussions, conducting research on competitor labels, and ensuring compliance with regulatory standards across different markets.

Novartis

Hybrid Permanent

Logistics Coordinator – Temperature-Controlled Supply (5 Month Secondment

This role involves supporting the day-to-day logistics activities for clinical studies, ensuring medicines are delivered on time and under the correct temperature conditions. You will manage temperature excursions, coordinate with logistics partners, and contribute to continuous improvement initiatives.

AstraZeneca Macclesfield, United Kingdom

On-site Contract

Associate Principal AI & ML Engineer – Evinova

As an Associate Principal AI & ML Engineer at Evinova, you will develop and integrate advanced algorithms and generative AI systems to optimize clinical trial design and improve drug development processes. Your role involves working with multi-source data, building production systems, and collaborating with cross-functional teams to drive impactful solutions.

AstraZeneca London, United Kingdom

Hybrid 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