Serve as the Responsible Person (RP/RPi) under EU Guidelines 2013/C 343/01, ensuring QMS implementation and GDP compliance; Act as the Management Representative for the UK market...
The Manager, will be responsible for preparing and/or overseeing regulatory submissions including the Clinical Trial Application (CTA), Marketing Authorisation Application (MAA),...
Lead development and revision of all MA Research procedural documents ensuring the procedural framework is updated promptly to reflect changes in scope and responsibilities...
Acts as a strategic partner across drug discovery, development, and commercial teams. Medical Writing participates in cross-functional drug discovery, development and commercial...
This role will provide strategic regulatory and scientific support on non-clinical and clinical development plans and work with both Regulatory Affairs – Strategic Project Leads...
Lead a group of scientists and is accountable for the development activities in the Process Development Team. Analyse Evaluate medicinal chemistry synthetic procedures to...
The Principal Scientist will take a lead role in the scientific development of all lab operational staff. Working with line managers develop training plans and material and deliver...