Senior Medical Writer

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

Key Responsibilities

Lead the preparation and review of clinical study reports, protocols, and 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

Required Qualifications and Education

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

Ability to work effectively in a dynamic environment and manage multiple projects

Experience in mentoring and guiding junior writers