The Director of Medical Writing will be responsible for generating high-caliber regulatory documents that align with strategic goals to support clinical development initiatives. This role involves overseeing document review procedures, collaborating with cross-functional teams, and ensuring adherence to international regulatory standards. Candidates should possess a bachelor’s degree in a scientific discipline and a minimum of 10 years of experience in regulatory medical writing within the pharmaceutical sector. Expertise in drafting intricate clinical documents and a background in oncology are strongly desired.
Summit Therapeutics provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
