Global Medical Writing Lead Regulatory Submissions

EMD Serono, Inc. is seeking a Senior Principal Medical Writer to lead end-to-end development of regulatory submission documents, ensuring scientific rigor, regulatory compliance, and timely delivery across global markets. You will serve as the primary writing lead within cross-functional teams, shaping strategy and timelines.

Hybrid role based in Billerica, MA with 3 days on site. You will mentor writers, drive best practices, coordinate with clinical, regulatory, pharmacovigilance, and

For the Global Medical Writing Lead for Regulatory Submissions position at EMD Serono, Inc., we are reviewing applications now.

Please review the full job details above before applying.

If your experience matches this role, we encourage you to apply.

All applications are reviewed carefully by our team.

The position is based in Billerica, MA, United States.

This opportunity is part of our work in Bio & Pharmacology & Health.