Angitia Biopharmaceuticals seeks a Sr. Manager/Associate Director, Regulatory Writing, to lead writing across its development programs from IND through lifecycle management.
You will plan, author, coordinate, and deliver submission-ready documents with strict timelines and high scientific standards. This role partners with Regulatory Affairs, Clinical Development, Biostatistics, Safety, and CMC, mentoring junior writers and managing external vendors while ensuring compliance with ICH, FDA, EMA
#J-18808-LjbffrSenior Regulatory Writing Lead Remote in workfromhome at Unknown Company
This position is listed as full time and onsite.