One of our research coordinators, Ben Connell, recently sat for (and passed!) the Association of Clinical Research Professionals (ACRP) exam for certification as a clinical research coordinator. To be eligible to take the exam, a clinical research coordinator must submit documentation that they perform the job duties of a clinical research coordinator and have performed a minimum number of hours in those duties. Some of those duties include: documenting adverse events, preparing or reviewing submissions to the Institutional Review Board (IRB), participating in conducting subject visits, maintaining source documents, and participating in the consent process.
With Ben’s addition as a CCRC, OCRI now has 7 total certified clinical research coordinators, and several more OCRI staff will be eligible to sit for the exam next year.
Congratulations, Ben!
Back
Essential cookies keep the site secure and functional. You can choose whether to allow non-essential cookies below.
Necessary
Required for security, navigation, and core site functionality. These always stay on.
Remember choices such as display preferences to improve your experience on return visits.
Help us understand how visitors use the site so we can improve performance and usability.
Support campaign tracking and embedded third-party tools that help us reach the right audience.
