Clinical Research Coordinator

Recruitment

Retention

Administrative Tasks

Chart review - onsite

Data entry and data migration

Assist with Study Visits, sample collection and processing - excluding venipuncture and study drug administration

Pre-screening for eligibility to protocol

Query Resolution

Study visit and audit preparation - monitoring visits

AE monitoring

Consenting

Scheduling and appointment reminders

Administrative tasks - maintaining study binder, regulatory filing, etc.

Source Document Creation

Regulatory document maintenance, preparation, and submission of study level IRB/Regulatory documents from approved templates