Senior Medical Writer – Regulatory & Clinical Documentation

A leading biopharmaceutical organization in North Carolina seeks a Principal Medical Writer to manage and lead the completion of various medical writing deliverables. Responsibilities include creating clinical documents, adhering to regulatory standards, and collaborating effectively with teams. A Bachelor's degree and 3-5 years of medical writing experience are required, along with strong project management and interpersonal skills. This role provides an opportunity to innovate and contribute to impactful therapeutic advancements. #J-18808-Ljbffr