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