Our coordination team consists of a pool of highly trained study coordinators that can assist the PI in coordinating some or all elements of a given study. They are skilled in activities such as identifying, screening, consenting and enrolling subjects, collecting and managing data, specimen handling, data entry, reporting adverse events and acting as a liaison with sponsors, hospital departments, the IRB and study participants. This team has experience in multiple disciplines, both adult and pediatric and is experienced in all phases of drug, device and pediatric trials, NIH funded and PI-initiated trials. The coordinators are all CITI, GCP, IATA and BLS trained.

Our coordination services are a fee for service in order to remove the total financial burden for PIs and their departments who would otherwise have to hire their own coordinators. We will charge an hourly rate for the time a coordinator works on a particular study. We are committed to subject enrollment, subject retention, patient safety and data integrity.

For more information

Teresa Arb RN, BSN, CCRC
Associate Director of Clinical Research