Senior Medical Writer & Regulatory Lead (Remote)

A leading life sciences consultancy is seeking a skilled Medical Writer in Raleigh, NC. The role requires at least 7 years of experience writing clinical and regulatory documents for drugs and devices. Responsibilities include managing clinical program documents, authoring high-quality deliverables, and mentoring junior writers. Candidates should possess advanced clinical research knowledge and expertise in FDA regulations. A collaborative team environment with opportunities for hybrid work is offered, alongside a commitment to diversity and inclusion. #J-18808-Ljbffr