Lead R&D Technical Writer

Job Summary

Working remotely on a contract basis, the Lead R&D Technical Writer will assist in the development and completion of clinical reports and other documentation while overseeing the electronic regulatory submission process.

Key responsibilities

• Assist in the timely development of clinical reports, summary documents, and package inserts
• Oversee the electronic regulatory submission process and provide recommendations for documentation formats and guidelines
• Ensure effective planning and management of timelines for all technical documents

Required qualifications

• Medical device experience is required
• A college degree or equivalent is necessary
• Minimum of 4 years of relevant work experience in technical writing
• Professional mastery of a specialized field of expertise
• Ability to work independently with minimal supervision