Clinical Trials Medical Writer

Role Overview

• Lead the development, revision, and maintenance of complex clinical study documents
• Serve as a subject-matter expert for medical documentation
• Manage multiple rounds of internal and external document review
• Participate in client interactions during study start-up activities

Requirements

• BA/BS, or equivalent experience in scientific field
• 1 yrs clinical trials or other laboratory experience required
• Applied knowledge of routine document content preparation
• Proficient in Microsoft Office and desktop publishing or word processing
• Education in medical or technical writing
• 1+ years’ experience drafting clinical trials documentation.

Benefits

• Health insurance
• 401(k)
• Paid time off
• Remote work options