Senior Principal Medical Writer

A company is looking for a Senior Principal Medical Writer to lead the development of clinical and regulatory documents.

Key Responsibilities

Develop and author clinical and regulatory documents, ensuring compliance with industry standards

Collaborate with cross-functional teams to gather and interpret clinical data

Mentor junior medical writers and review documents for consistency and regulatory adherence

Required Qualifications

A master's degree or Ph.D. in Life Sciences, Medicine, or a related field

Extensive experience in medical writing within the pharmaceutical or biotech industry

Demonstrated leadership skills with experience in managing and mentoring teams

Strong proficiency in scientific writing and editing

Detail-oriented with strong organizational skills to manage multiple projects