Medical Writer

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