Clinical Trials Medical Writer

Job Summary

A company is looking for a Clinical Trials Medical Writer.

Key Responsibilities

• Lead the development, revision, and maintenance of clinical study documents in accordance with SOPs and regulatory requirements
• Serve as a subject-matter expert for medical documentation throughout the study lifecycle and manage document reviews
• Maintain knowledge of relevant regulations and participate in client interactions during study start-up and amendments

Required Qualifications

• BA/BS or equivalent experience in a scientific field
• 1 year of clinical trials or laboratory experience required
• Applied knowledge of document content preparation and regulatory guidance
• Proficient in Microsoft Office and desktop publishing or word processing
• Education in medical or technical writing is preferred