A biopharmaceutical company is looking for an Associate Director of Scientific and Medical Writing to lead HIV-focused regulatory writing activities. This role entails managing program-level writing efforts, overseeing the planning and production of clinical documents for global submissions, and leading matrix teams to ensure compliance with regulatory requirements. Candidates should possess a PhD, PharmD, MPH, or MS, have experience in regulatory submissions, and leadership in the life sciences domain. Exceptional communication skills are also essential. #J-18808-Ljbffr