Principal Medical Writer

A company is looking for a Principal Medical Writer to lead the development of high-quality regulatory and clinical documents remotely.

Key Responsibilities

Lead the preparation and review of clinical study reports, protocols, and other regulatory documents

Collaborate with cross-functional teams to gather and synthesize information for document development

Mentor and train junior medical writers while ensuring adherence to regulatory requirements and standards

Required Qualifications

Advanced degree in life sciences, medicine, or a related field; relevant certifications preferred

Significant experience in medical writing, particularly in regulatory submissions and clinical documentation

Strong understanding of regulatory requirements and industry standards for clinical writing

Exceptional writing and editing skills with a keen eye for detail

Commitment to maintaining high standards of quality and compliance in all medical writing activities