Angelena Dababneh

Angelena Dababneh is a Regulatory Affairs Coordinator III with extensive experience in supporting FDA submissions, IND trials, and sponsor-initiated studies. She oversees the full lifecycle of clinical trials—from start-up through close-out—managing regulatory compliance and documentation across all phases. Her responsibilities include preparing and submitting amendments, IRB and FDA applications, and maintaining accurate regulatory records to ensure adherence to federal guidelines and sponsor requirements.