Ha Hong Van
I am a Clinical Research Associate with 4 years of experience in clinical trials, including managing complex multiple
sites clinical trials. Skilled in project management, data monitoring and analysis, ethics submission, reporting,
and adherence to ICH-GCP standards. Highly effective communicator with demonstrated success supporting
clinical research delivery, stakeholder management, and ability to build effective relationships across multidisciplinary
teams.
Abstracts this author is presenting:
