- Full-time · Associate
- 2+ years
Supports the Clinical Trial Patient Safety Organization by evaluating and ensuring the quality of clinical trial patient safety data.
Responsibilities
- Provides timely assessment of reported clinical trial data
- Participates in safety surveillance activities
- Reviews and analyzes safety-related data
- Maintains audit readiness
- Monitors safety queries to investigators
Requirements
- Bachelor's degree with related health science background
- Nice to have: RN experience
- Nice to have: clinical pharmacy experience