Lead Medical Writer - Regulatory Submissions

A biopharmaceutical solutions organization is seeking a Principal Medical Writer to lead the medical writing process. This role involves managing and completing a variety of important documents related to clinical studies, ensuring clarity, accuracy, and adherence to regulatory standards. The ideal candidate will have 3-5 years of relevant experience, a strong understanding of FDA and ICH regulations, and excellent communication and project management skills. A supportive environment focusing on career development is offered.