Senior regulatory affairs CMC manager ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our
Your work will change lives. Including your own. The Impact You’ll Make You will join an innovative and passionate clinical development team dedicated to improving the lives of patients suffering from devastating diseases. You will lead
Your work will change lives. Including your own. The Opportunity At Recursion we are redefining drug discovery by uniting industrial-scale data generation with sophisticated computational models. We are seeking a visionary Head of DMPK to join
Job Description SummaryThe Clinical Development Director (CDD) is the clinical/scientific expert and if assigned the clinical development lead of a section of a global clinical program and/or trial. (e.g., an indication, a new formulation, or a
About the Trust Were one of the UK’s biggest charities and we care for 2,000 miles of canals, rivers, docks and reservoirs because we believe life is better by water. Were looking for people who support
About the Trust Were one of the UK’s biggest charities and we care for 2,000 miles of canals, rivers, docks and reservoirs because we believe life is better by water. Were looking for people who support
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join us as a Medical Director M-SERM - And lead our efforts in medical safety evaluation and risk management. What You’ll Do: • Maintain understanding of methods for recording
The Role: The Associate Director, CMC Regulatory Science-International will be based at the Harwell, UK site and as part of a team be responsible for preparing and overseeing CMC and Quality related agency correspondence and regulatory
Do you want to use your strong analytical, problem-solving skills to help find treatments for rare disease patients? About Healx Healx is an AI-powered tech bio company that is redesigning drug discovery. With 10,000 rare diseases
BandLevel 5 Job Description SummaryOffice Location: London (The Westworks), United Kingdom #LI-Hybrid Hybrid (12 days per month on-site if living within 50 miles to our London office) #LI-Remote Remote (if living beyond 50 miles to our
Your work will change lives. Including your own. The Impact You’ll Make Lead development and implementation of CMC regulatory strategy for small molecule investigational drugs in global Phase 1-3 clinical trials and marketing applications. Influence the
Overview IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the product lifecycle. The Patient Centered Solutions (PCS) Strategic & Scientific Research (SSR) team leads the industry in generating
The Role Moderna is looking for a Associate Director, CMC Regulatory Affairs-International, to join our team based in London, UK. This pivotal role will focus on preparing and overseeing CMC and Quality related agency correspondence and
Regulatory Affairs Project Manager Location: Swindon Position summary; Monday – Friday; 09.00 – 17.00 onsite. The Regulatory Affairs function ensures the organisation remains compliant with all applicable regulations and legislation, while actively engaging with federal, state,
Overview General Operative – Injection DepartmentLocation: Corby, UKPay: £13.45 per hour Shift - AM (Monday to Thursday 6am to 2pm & Friday 6am to 11:30am) Full-time, Permanent | 37.5 hours per week Are you hands-on, detail-oriented,
About the Trust Were one of the UK’s biggest charities and we care for 2,000 miles of canals, rivers, docks and reservoirs because we believe life is better by water. Were looking for people who support
Salaryto share the workload between 2 mechanics in the elgin Depot We are looking for experienced Backshift PCV mechanic to join our Elgin team. Earnings of £20.78 per hour Guaranteed 45 hours minimum with overtime potentially
Associate Director/Director, Pharmacometrician Step into a role where science meets strategy and your expertise shapes the future of drug development. As an Associate Director(AD)/Director, Pharmacometrician, you’ll lead high-impact modeling and simulation efforts within a dynamic Clinical
Business Introduction At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines,
We are seeking a UK‑based Site Start-Up (SSU) Specialist to join our high‑performing and collaborative team, supporting the delivery of early‑phase clinical trials (Phase I and Phase Ib). This role plays a critical part in enabling