Job Title: Senior Regulatory Affairs Officer Location: Reading, UK Working Pattern: 3 days onsite in Reading, 2 days remote per week About This Job As Senior Regulatory Officer - Promotional & Non-Promotional Materials Review within our UK and
Regulatory Science and Policy Associate - VIE Contract Location: United Kingdom, Reading Target start date: 01/10/2026 iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged
The RPM will provide business support to GRA. Key member of the Project Management Team ensuring the Product strategy aligns with the Regulatory strategy and works in concert with the PMT and GRT to operationalize the plans.
Job Level: Senior Director, Drug Development Location: Home-based in Europe Job Overview: Manages a department or small unit.; Provide leadership and advice on the development of optimum strategies for drug development, product lifecycle management and portfolio
Job Overview Acts as Lead Medical Writer on most types of writing projects. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Performs Senior Review
Principal Medical Writer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are
Medical Director Neuroimmunology ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are
Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates in South East England. Why IQVIA? Career development opportunities to grow
Job LocationREADING TECH CENTER Job Description Ready to fuel the success of globally renowned brands that millions of consumers can’t live without? Ready for career where you are fully supported by world-class training and development to
Senior Clinical Editor ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are
Reports to: Elizabeth Hims – NERC Operational Safety Assurance Manager (Aviation & Maritime) Base Location: AAP locations rotate between stakeholder sites in Cambridge, Swindon and London. Salary: £4800-£6000 per year based on experience Duration/Contract type: An
Cambridge (England) Senior Clinical Trial Associate to start ASAP! ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation,
UC Architect CPS has successfully built one of the UKs Microsoft solutions practices. We are a long-established and highly respected Microsoft partner with an extensive portfolio of high-profile clients that continues to grow. Due to our
Department: IT Reports to: Associate Director of IT and Change Salary: £40,000 to £45,000 DOE Location: Can be based at either Reading or Salford (hybrid) The Opportunity We’re looking for a hands-on Business Analyst to support
The Trial Delivery Leader (TDL) serves as the single point of accountability for trial operational strategy, trial-level budget, quality, and on-time delivery of assigned clinical trials. This role represents the evolution of the Global Trial Leader
Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates. Why IQVIA? Career development opportunities to grow as we grow AI‑powered
IVDR Study Start-Up Associate - UK ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility,
Regulatory Science and Policy Associate - VIE Contract + Location: United Kingdom, Reading + Target start date: 01/10/2026 iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and
Job Title: Senior Regulatory Affairs Officer - Promotional & Non-Promotional Materials Review Location: Reading, UK Working Pattern: 3 days onsite in Reading, 2 days remote per week About This Job As Senior Regulatory Officer - Promotional & Non-Promotional
Director Regulatory Affairs ICON plc is a world-leading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape