A global biopharma company is seeking an Associate Director of Medical Writing to prepare high-quality regulatory documents. The candidate will work with cross-functional teams to align on communication points and oversee writers. A minimum of 8 years of experience in the pharmaceutical industry is required, alongside exceptional written communication skills. This role involves managing multiple projects and requires knowledge of ICH and CTD guidelines. The compensation range for this position is competitive, reflecting the candidate's experience and qualifications. #J-18808-Ljbffr