Clinical Research Associate
CurrentManaged subject compliance for 2-3 simultaneous studies with 150+ subjects per study• Briefed 10+ sites weekly about 3 study requirements compliance and reports per subject with 25+ subjects per site• Educated 1,000+ subjects on study requirements, recordings, technology use and collection schedules• Led weekly virtual meetings with 2-3 cross-sponsor organizations per meeting• Consistently maintained over 70% TTM compliance, 95% Holter recordings and 85% for 12-lead reports as study lead• Trained virtually 50+ sites globally on trial processes and medical technology directly impacting subjects’ success infulfilling 3 main study requirements• Supervised 3-4-person study team for 400+ participant study across 20+ sites• Conferred with internal senior leadership about study strategy and logistics