Clinical Research Center


The CRC provides the following services:

Marketing of services to potential study sponsors and referrals to our physician investigators

Clinical trial placement with physician investigators

Marketing of trial opportunities to potential subjects

Study initiation and regulatory maintenance

    • Contract and budget preparation, regulatory documentation preparation and maintenance including IRB submission and continuing review

Coordinator study support

    • Patient screening, enrollment, randomization
    • Coordination of all study procedures (i.e., study visits, study drug administration, study-related interventions per study protocol)
    • Availability for all sponsor monitoring visits and audits

Data management

    • Completion of case report forms, query resolution
    • Reporting adverse events and other regulatory requirements to the IRB
    • Database entry