Lead Analyst, R&D Technical Writing

Job Summary

Working remotely on an 18-month contract, the Lead Analyst, R&D Technical Writing will assist in the development of clinical reports and regulatory submissions while overseeing documentation formats and guidelines.

Key responsibilities

• Assist in the timely development and completion of clinical reports, summary documents, and package inserts
• Oversee the electronic regulatory submission process and provide recommendations for documentation formats
• Ensure effective planning and management of timelines for all aspects of 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 in a specialized field of expertise
• Ability to work independently with minimal supervision