Principal Medical Writer

Job Summary

A company is looking for a Principal Medical Writer.

Key Responsibilities

• Lead the preparation, review, and editing of clinical study documents, ensuring compliance with regulatory guidelines
• Collaborate with cross-functional teams to analyze clinical trial data and communicate scientific findings
• Mentor junior medical writers and contribute to the development of publication plans and manuscripts

Required Qualifications

• Advanced degree in Life Sciences, Pharmacy, Medicine, or related field
• Minimum of 5-7 years of experience in medical writing within the pharmaceutical or CRO industry
• Strong understanding of regulatory requirements governing clinical documents
• Proficiency in interpreting complex clinical trial data and scientific research findings
• Demonstrated ability to manage multiple projects in a fast-paced environment