Hybrid in Boston, Massachusetts
•
Today
Duration:2 months, with potential to extend/convert Schedule:40 hrs/weekRelocation:Full relocation package available Key Responsibilities: Lead medical writing activities for clinical and regulatory submissions.Independently author complex clinical and regulatory documents.Coordinate clinical sections of complex regulatory filings and MAAs.Provide strategic guidance across clinical programs and cross-functional teams.Lead/manage Medical Writing Science team activities and staff development.Drive
Easy Apply
Contract
95
