Bluestone Clinical Operations Team
A group of specially-trained clinical operations professionals and full-time dedicated staff assists investigators and sponsors to successfully complete their trials.
Bluestone Clinical Research Coordinators (CRCs) work in a team environment under the direction of Principal Investigators. Their responsibilities include: recruiting support, screening and enrolling clinical study participants; arranging follow-up visits; maintaining and dispensing drug and other study supplies; completing and ensuring the accuracy of case report forms and regulatory documents; and ensuring the adherence to Good Clinical Practice guidelines.
The research recruitment specialist oversees all clinical research subject recruitment efforts in the Bluestone Center for Clinical Research. This includes preparation and IRB approval of all recruitment materials: written flyers, brochures, pamphlets, newspaper ads, electronic bulletin board notices, e-mail messages, letters to referring practitioners; radio advertisements; television advertisements.
Bluestone also prepares and analyzes weekly recruitment updates for all Bluestone-supported investigations to help track the progress of study subject recruitment and retention.
As an integral member of the Bluestone biostatistics section, the database manager coordinator provides guidance on the development of
Computer Recorded forms (CRFs), data management software and data base design, oversight on data entry, cleaning and general discrepancy analysis.
|
