Senior Medical Writer

The role

You'll lead the completion of medical writing deliverables for clinical studies, including protocols, clinical study reports, patient narratives, and regulatory submissions like NDAs and eCTDs. Working with clients, biostatistics, data management, and regulatory affairs teams, you'll coordinate document reviews, mentor junior writers, and ensure compliance with ICH E3 guidelines and company standards. This is a senior-level full-time remote position with minimal travel (less than 25%).

Tools and skills