As an Associate Medical Writer, you'll engage in the moderation of discussions for developing study protocols and reports, facilitate document reviews, maintain audit readiness, conduct literature searches, and contribute to internal and external medical activities. You will collaborate with global medical directors and maintain strong relationships with stakeholders while improving teamwork and sharing practices.

The Principal Medical Writer independently manages the preparation of written deliverables required for clinical development and regulatory submissions. This role involves collaborating with cross-functional teams to provide strategic input on study designs, analyzing study plans, and mentoring junior writers.