Medical Writer - Remote

Overview

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.

In Short

• Analyze and interpret safety results of clinical trials.
• Compile, write and edit clinical study reports and other industry documents.
• Confirm accurate classification of events and medications using standardized coding systems.
• Review/evaluate study results to determine if safety objectives were met.
• Perform peer QC function of safety text prior to inclusion in the CSR.
• Ensure quality and on-time delivery of scientific reports.
• Use technology to work with international teams.
• Lead project-related client communication.
• Interact with internal departments.
• Participate in functions to ensure department success.

Requirements

• Bachelor's degree in a medical or scientific field or equivalent experience.
• 1-3 years experience in a hospital/clinical setting.
• Professional writing and editing skills for accurate reporting.
• Detail-oriented, thorough, and methodical.
• Ability to work independently and under pressure.
• Excellent communication/interpersonal skills.
• Knowledge of medical, pharmaceutical, and/or clinical research concepts preferred.

Benefits

• Work remotely from anywhere in the United States.
• Opportunity to contribute to innovative clinical research.
• Collaborate with a multi-disciplinary scientific team.
• Engage in a dynamic and fast-paced work environment.