Medical Writer
RemoteUnited States
EXPIREDUnited StatesRemoteFull TimeLarge
Full TimeLarge
Job Summary
Analyze and interpret safety results from clinical trials, including vital signs, adverse events, and diagnostic procedures. Compile, write, and edit Phase I and Phase II clinical study reports, stand-alone safety narratives, and synoptic CSRs. Perform peer quality control on safety text, review reports for completeness, and ensure deliverables comply with Good Clinical Practice and regulatory standards. Lead project-related client communication and collaborate with internal departments to ensure on-time delivery of scientific reports. Work remotely using technology tools like Veeva and Microsoft 365.
Required Qualifications
- Bachelor's degree and/or professional license in a medical or scientific field (RN, BS, RPh, MS, MPH)
- 1-3 years experience in hospital/clinical setting or interpreting medical or clinical results
- Professional writing and editing skills for accurate and concise reporting of clinical trial results
- Ability to interpret and present data in preparing a coherently written document
- Detail-oriented, thorough, and methodical
- Ability to work without close supervision
- Ability to work under pressure
- Ability to multi-task and to respond rapidly to changing priorities and aggressive timelines
- Excellent communication/ interpersonal skills
Desired Qualifications
- Knowledge of medical, pharmaceutical, and/or clinical research concepts
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