R&D Technical Writer

Job Summary

Working remotely on a contract basis, the R&D Technical Writer will lead the development of clinical reports and regulatory documents while managing timelines with precision in a fast-paced medical technology environment.

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 and guidelines
• Ensure effective planning and management of timelines for all technical documents while working independently

Required qualifications

• Minimum of 4 years of relevant experience in technical or regulatory documentation
• Professional mastery of a specialized field of expertise
• College degree or equivalent experience
• Strong attention to detail in technical evaluations and document development