With nursing, nutrition research, and laboratory support cores, the Clinical Research Center (CRC) staff provide Ohio State investigators with the cutting-edge tools and services needed to explore important clinical questions as well as the pathophysiology and treatment of disease.
The CRC has been continuously providing clinical research services since 1960. Staff currently collaborate with investigators to implement around 100 active research protocols at any given time.
CRC Core Services
New Study Workflow
Timeline: Before grant submission
- Step 1: Enter CRC Resource Request
CRC Resource Request
Timeline: After grant funded, 4-6 weeks prior to start of recruitment
- Step 1: Complete Electronic CRC Application (CRC Application)
- Step 2: Meet with CRC staff assigned to project; answer questions, work out details
- Step 3: Confirm all CRC documents are approved and notify CRC staff when ready to begin recruitment
Timeline: Participant recruitment
- Schedule participants
- Follow CRC scheduling guidelines (guidelines listed in section below)
- Parking information for participants
- Directions to CRC for participants
Timeline: Ongoing
- Notify CRC of changes to CRC protocol implementation
- Send CRC staff updated revisions of protocol documents and IRB/WIRB approvals
Timeline: End of Participant Enrollment
- Notify CRC Nurse Manager when the study is done with enrollment to start study close-out procedures.
CRC Scheduling Guidelines
NOTE: All PHI must be sent securely or via an OSUMC email account.
The following is a guideline to assist you when scheduling research participants on the CRC.
- Email Claire and Holly the following information, putting the CRC study name in the subject line.
- Study name (ex. NEURO155)
- Study visit type/definition (ex. V1 Day 2)
- Desired visit date and time
- Participant name
- Participant study subject number
- If you are scheduling a new participant who has not been at CRC before, the following additional information is required:
- Full name (Please confirm the correct spelling with the participant)
- DOB
- Sex assigned at birth
- MRN – some studies do not require a hospital MRN and a unique identifying number can be created. This will be discussed and created prior to the first participant starting the study.
Important: Please email both Claire and Holly when you send scheduling requests.
Please do not hesitate to contact Claire or Holly if you have any questions or concerns.
Claire Carlin
Sr Clinical Research Coordinator
Phone: 614-293-6182
Email: claire.carlin@osumc.edu
Holly Bookless
CRC Nurse Manager
Phone: 614-293-8749
Email: holly.bookless@osumc.edu