Medical Writer

Job Summary

Working remotely in a full-time capacity, the Medical Writer will analyze and interpret safety results from clinical trials, compile and write clinical study reports, and ensure compliance with regulatory standards.

Key responsibilities

• Analyze and interpret various medical results, including vital signs and clinical laboratory values, to compile Phase I and II clinical trial documents
• Review and evaluate study results to determine the accuracy of safety objectives and ensure quality and on-time delivery of scientific reports
• Lead project-related client communication and interact with internal departments to support the success of the team

Required qualifications

• Bachelor's degree or professional license in a medical or scientific field (RN, BS, RPh, MS, MPH) or equivalent experience
• 1-3 years of experience in a hospital or clinical setting, interpreting medical or clinical results
• Professional writing and editing skills for accurate reporting of clinical trial results
• Detail-oriented with the ability to work independently and under pressure
• Knowledge of medical, pharmaceutical, and clinical research concepts preferred