Responsibilities Include:
- Selecting and coding adverse events
- Determine seriousness of AEs, writing/editing case narratives
- Perform labeling assessments
- Requesting follow-up information when needed
- Adhere to regulations, guidelines, Standard Operating Procedures, data entry and writing practices
Qualifications:
- Bachelor’s Degree
- 4 to 7 years of experience in Quality Assurance and Quality Control
- HCP is required
- Drug Safety experience is desired
