Lead Medical Writer & Regulatory Submissions Expert

A leading clinical research firm in Charleston is seeking a Senior Medical Writer to manage the creation and editing of clinical documents. The role includes project management, quality control, and client interaction, requiring strong organizational, communication, and leadership skills. Qualified candidates should possess a Bachelor's degree in Life Sciences and demonstrate expertise in clinical regulatory documentation and project management. This opportunity offers a fast-paced environment with a focus on collaboration and client satisfaction. #J-18808-Ljbffr