Lead the nonclinical DMPK strategy and design the appropriate studies to fulfil regulatory requirements Work with colleagues globally to resolve project-related ADME challenges Author high quality regulatory documents including INDs, CTAs and NDA filings Educated to PhD in a scientific related discipline Minimum 5 years industry experience contributing to drug discovery projects with a track record of moving small molecules from target validation to first in humans
Senior Project Coordinator, Regulatory in City of London employer: RBW Consulting
Join a dynamic healthcare manufacturing site in Trefriw, North Wales, where you can make a significant impact as a Laboratory Supervisor. We offer a supportive and collaborative work culture that prioritises professional growth, with opportunities to lead a dedicated team and influence quality standards. Enjoy a competitive salary, career development prospects, and the chance to work in a beautiful location while contributing to meaningful advancements in laboratory science and compliance.
