Pace is seeking a Senior Regulatory Affairs Specialist (Remote) to lead global CMC regulatory strategies. You will author and compile CMC sections for INDs, IMPDs, CTAs, amendments, and reports, and draft Module 2/3 documents with precision.
Ideal candidates bring 10+ years in CMC/regulatory affairs, strong documentation skills, and experience interfacing with FDA/EMA/PMDA. Includes a comprehensive benefits program for full-time staff.
#J-18808-LjbffrSenior Regulatory Affairs Lead - Remote, Global Submissions in workfromhome at Unknown Company
This position is listed as full time and able to be worked remotely.