Offer summary
Qualifications:
Bachelor's degree in medical/scientific field, 1-3 years experience in clinical setting, Professional writing and editing skills, Ability to interpret medical data, Knowledge of clinical research concepts preferred.Key responsabilities:
- Analyze and interpret clinical trial results
- Compile and write clinical study reports
- Perform peer QC function for safety text
- Ensure compliance with regulatory standards
- Communicate proactively with multidisciplinary team