Clinical Research Coordinator
Current• Lead recruitment efforts in screening potential patients while focusing on retention in active studies• Obtain and document informed consent as approved by the IRB and greenlit by the sponsor• Create CRFs by inputting study data into electronic data capture systems• Manage and ensure completion of study activities per protocol for >15 Genentech/ Roche, Janssen, Kodiak, and Iveric Bio ophthalmic clinical trials• Maintain compliance with GCP, 21 CFR, ICH, and IATA guidelines