Senior Medical Writer — Regulatory Submissions Lead

A global biotechnology company is seeking a Senior Medical Writer to manage the preparation of clinical study documents and ensure compliance with regulatory submissions. This role requires advanced medical writing experience and a strong understanding of drug development processes. The position involves collaboration with cross-functional teams and the ability to lead document preparation efforts. Ideal candidates will possess excellent communication skills and regulatory knowledge to support impactful medical writing efforts. #J-18808-Ljbffr