Lead Analyst, R&D Technical Writing

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