Medical Writing Manager

This manager-level medical writing role supports Global Development and partners with clinical, regulatory, biostatistical and other cross-functional teams. As lead writer and primary contact for assigned compounds, it coordinates clinical and regulatory documents across therapeutic areas, shaping content and scientific strategy. The role also contributes to therapeutic-area planning and process working groups. Work includes setting document timelines, leading planning and review meetings, coordinating contributors and overseeing contractors when needed. The manager guides colleagues on writing processes, mentors junior writers and recommends process improvements. The role calls for independently interpreting and accurately presenting complex statistical and medical information, resolving most issues independently and applying guidance such as ICH requirements. Applicants need a scientific university or college degree, at least eight years of relevant pharmaceutical or scientific experience, and at least six years of clinical or regulatory medical writing experience. Strong oral and written communication, attention to detail, leadership and time-management skills are also required.