Clinical Research Coordinators (CRC)

Left to right:
Krystallia Kalliontzi, Alice Siqueira, Donald Garmon, Dinah Neri, Erica Queiroz, Monika Epler, Lena Nemelivsky,
Emmanuela Mathurin

Bluestone's Clinical Research Coordinators (CRCs) are specialized research professionals responsible for the organization, coordination, and overall integrity of all research projects at the center.

Principals and co-investigators provide the overall direction in our clinical study, but our experienced CRCs have significant roles in the following clinical research activities:
– Protocol development
– IRB, FDA applications and compliance
– Recruiting research participants
– Screening and enrolling participants
– Obtaining participant informed consent
– Scheduling tests and procedures
– Collection of clinical research data
– Ensuring accuracy of documentation
– Dispensing study medications
– Managing the use of investigational devices
– Maintaining databases