Latest clinical research associate Jobs

Regulatory Transparency (Disclosures) Professional

In this role, you will manage the end-to-end execution of clinical trial registration and results posting, ensuring Roche complies with global regulations. You will lead the accurate and timely posting of clinical trial data, manage cross-functional teams, and ensure consistency and quality in all submissions.

Roche Welwyn Hatfield, United Kingdom

On-site Permanent

Disease Area Lead - Hepatology, Renal and Cardiovascular diseases

Leads clinical operations strategy and delivery across Hepatology, Renal, and Cardiovascular disease portfolios within GSK’s R&D engine. Oversees end-to-end development from early phase through life-cycle management, driving operational excellence, team development, and cross-functional alignment. Champions data-driven decision-making, risk management, and innovation adoption to accelerate high-impact assets.

GSK Stevenage, United Kingdom US$242,550 – US$404,250 pa

Hybrid Permanent

Head of RTSM (Randomization and Trial Supply Management)

This role involves leading the RTSM function, partnering with clinical development, operations, quality, and external vendors to design and deliver patient-focused randomization and clinical supply solutions. Responsibilities include managing cross-functional teams, ensuring on-time randomization and supply availability, and improving RTSM processes and governance.

GSK Stevenage, United Kingdom

Hybrid Permanent

Disease Area Lead - Hepatology, Renal and Cardiovascular diseases

Lead clinical operations strategy for Hepatology, Renal, and Cardiovascular disease portfolios, driving end-to-end delivery from early phase through life-cycle management. Oversee a matrix team, align operational execution with R&D goals, and champion data-driven decision-making and innovation in clinical development. Shape culture, manage risks, and ensure inspection readiness across global assets.

GSK Canterbury, United Kingdom US$242,550 – US$404,250 pa

On-site Permanent

Statistics Director, Oncology

This role involves leading statistical strategies for key oncology programs, designing robust clinical trials, and mentoring statisticians. The position emphasizes innovation, regulatory interactions, and cross-functional collaboration to advance the development of new cancer therapies.

GSK Stevenage, United Kingdom

On-site Permanent

Statistician (Scientist)

The role involves providing statistical support for manufacturing and analytical processes, using advanced data analytics and visualisation techniques. You will work across multiple teams to improve process understanding and drive data-driven decision-making, contributing to AstraZeneca's digital transformation.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent

Supply Planner

The Supply Planner ensures uninterrupted production by managing raw material procurement and inventory across clinical and commercial manufacturing operations. This role involves running MRP processes, maintaining inventory policies, coordinating with suppliers and 3PLs, and leading supply continuity efforts. The position works cross-functionally with finance, quality, and manufacturing teams to align supply plans with demand forecasts and resolve supply chain disruptions.

Autolus Stevenage, United Kingdom

Hybrid Permanent

NPI Launch Lead

This role leads the logistics and project management for new pharmaceutical and consumer product launches at GSK’s Barnard Castle site, ensuring timely, compliant market rollouts. The NPI Launch Lead coordinates cross-functional teams, manages launch timelines across global markets, and ensures adherence to GMP, quality, and regulatory standards throughout the product introduction lifecycle.

GSK Barnard Castle, United Kingdom

Hybrid Permanent

Global Studies Asset Manager (GSAM)

The Global Asset Study Manager (GASM) at Roche/Genentech is responsible for the efficient execution of global clinical trials, ensuring consistency and compliance with IHC-GCP and Roche processes. Key responsibilities include coordinating study management, developing essential documents, driving innovation, and maintaining inspection readiness.

Roche Welwyn Hatfield, United Kingdom

On-site Permanent

Regulatory Affairs Manager

Regulatory Affairs ManagerType: PermanentLocation: Pancras Square, LondonIntroduction to roleDeliver and maintain competitive licences for the UK, driving regulatory strategy for new initiatives and ensuring regulatory compliance for defined product and project responsibilities, including project leadership. Achieve timely delivery of clinical...

AstraZeneca London, United Kingdom

Senior Principal Statistician

This role involves providing advanced statistical expertise to support oncology clinical development across all phases, from early-stage trials to late-phase studies. The Senior Principal Statistician will lead the design and analysis of clinical trials using innovative methodologies such as Bayesian statistics and simulation techniques, working closely with cross-functional teams. The position emphasizes methodological innovation, risk assessment, and decision-making support within a global biopharma environment.

GSK Stevenage, United Kingdom

Hybrid Permanent

Director, Process Engineering & Packaging

Leads process engineering and packaging for biologics at AstraZeneca, driving development of clinical and commercial drug product processes including fill/finish, device assembly, and packaging. Manages a team of scientists and engineers, oversees technology transfer across internal and external manufacturing sites, and advances design for manufacturability and regulatory strategies. Focuses on innovation, scale-up, and technical excellence within a global biopharmaceutical manufacturing network.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Senior Statistician I

The Senior Statistician I will lead statistical input into clinical and preclinical study design, analysis, and reporting within AstraZeneca’s CVRM team. This role involves developing robust statistical analysis plans, applying modelling and simulation techniques, and translating complex results into actionable insights for multidisciplinary teams. The position emphasizes methodological rigor, regulatory readiness, and collaboration across global therapy areas to accelerate evidence generation for innovative medicines.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Lead Patent Paralegal

Work with usOur team are passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and Autoimmune disease to deliver life-changing treatments to patients.Whilst working at Autolus you will enjoy a flexible, diverse and dynamic working...

Autolus London, W12 7RH, United Kingdom

SERM Scientific Director, Oncology

The SERM Scientific Director role involves leading pharmacovigilance and risk management strategies for clinical development and post-marketing products. Responsibilities include evaluating safety data, managing safety concerns, and supporting regulatory activities. The role operates in a global, cross-functional environment and may include mentoring responsibilities.

GSK United Kingdom

Hybrid Permanent