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