Job description
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.
