We assist both new and experienced investigators with the review, preparation, and conduction of industry-sponsored and investigator initiated clinical research.
- study feasibility
- logistical considerations
- budgetary review and negotiation
- financial management
Experienced, certified clinical research coordinators are available, both on and off site, to provide complete study coordination or a range of services, such as, IRB preparation and submission, study start-up, regulatory compliance, participant recruitment, and data management.
Krista Garrison, MPH, CCRP
Interim Director, Clinical Trials Office