Senior Medical Writing Manager

Leading a team of medical writers, the full-time Senior Medical Writing Manager will be responsible for developing regulatory documents and ensuring compliance with industry standards in a remote setting.
Key responsibilities

Manage the preparation and review of clinical study reports, protocols, and other regulatory submissions
Oversee the medical writing team, providing guidance and mentorship to ensure high-quality deliverables
Collaborate with cross-functional teams to support project timelines and regulatory requirements

Required qualifications

Advanced degree in life sciences, medicine, or a related field
Significant experience in medical writing within the pharmaceutical or biotechnology industry
Proven track record of managing teams and projects effectively
In-depth knowledge of regulatory guidelines and industry standards
Experience with clinical trial documentation and submissions