Design and maintain electronic source documents and regulatory binders primarily using CRIO and other CTMS platforms. Translate study protocols into compliant templates and align study procedures with financial tracking and budgets.
Responsible for accurately entering and verifying clinical trial data into Electronic Data Capture (EDC) systems. The role involves performing quality checks and collaborating with research coordinators to resolve data discrepancies.
Conduct outreach and pre-screen potential participants for clinical trials via inbound and outbound calls. Educate patients on study protocols and maintain accurate records in the recruitment tracking system.
Identify, qualify, and schedule potential participants for Central Nervous System clinical research studies through inbound and outbound calls. Document all interactions in recruitment systems while ensuring compliance with IRB and HIPAA regulations.
