I will review and coordinate tasks in clinical trials, including performing:
- Clinical research.
- Medical records review.
- Adverse event detection.
- Reporting to managers.
- Managing clinical research teams.
I will provide:
- Daily/weekly reports.
- Constant communication (during agreed-upon working hours)
I have worked on similar projects with:
- Big pharma companies such as IQVIA and Roche (for adverse events detection).
- Clinical trials (for adverse events and drug effect detection).