CRA Training Academy
Clinical Research Training & Internship covering C
ATLANTA, GA
12.2019 - 10.2020
- Monitored safety events reported during the course of clinical trials in accordance with SOPs.
- Monitored site activities and sent follow-up letters to participants.
- Assessed records of each patient, reviewed databases and checked referrals to locate potential research study participants.
- Collaborated with sponsors and investigators to carry out efficient and fully compliant research trials.
- Attended meetings and reported on activities and resolutions.
- Assessed incoming source documentation for accuracy and completeness against case report forms.
- Achieved project-specific quality and performance standards and provided documentation and communication.