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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.
STEMHUNTER is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, sexual orientation, gender identity, and gender expression), national origin, age, disability, genetic information, veteran status, or any other status protected by applicable federal, state, or local law. We comply with all applicable equal employment opportunity and affirmative action regulations.
