Clinical Research Associate
Wake Research
05.2023 - Current
- Reviewed clinical data, source documentation, case report forms and investigative site regulatory files to verify accuracy and completion.
- Adhered to procedures, practices and regulatory requirements to maintain health, safety and environmental compliance.
- Implemented electronic data capturing systems to adhere with clinical research guidelines.
- Conducted initiation, monitoring and closeout visits to verify study procedures, regulatory documents and data completion.
