Senior Regulatory Medical Writer — Lead Clinical Submissions
A leading clinical research organization is seeking an experienced Medical Writer to evaluate and interpret clinical literature, write regulatory documents, and mentor team members. The ideal candidate has 3-5 years of experience in regulatory and clinical medical writing, along with strong organizational and writing skills. This role involves interacting with clients and managing project timelines, contributing to the production of high-quality medical documents that support life-changing therapies. The position is based in Raleigh, North Carolina.
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