Research Roadmap: Navigating the CIRB Process
See flyer here
Purchase contact hours here
Ms. Sarah Stutler, MBA, CCRP
11:30 am –12:00 pm –Lunch Provided
12:00 pm – 1:00 pm – Educational Presentation including Q&A
1:00 pm – 1:30 pm – Networking 1:1 with speaker
Program Description: West Virginia University (WVU) Human Research Protection Program Intuitional Review Board (IRB) Coordinator, Ms. Sarah Stutler will be providing guidance for researchers to follow when using a Central Intuitional Review Board (CIRB) when conducting research at WVU. The CIRB workflow will be discussed in detail to ensure full compliance with WVU IRB policies and procedures.
Upon completion of this Seminar, attendees should be able to:
- Demonstrate knowledge of the Central Institutional Review Board (CIRB) Workflow for West Virginia University
- Describe the requirements for CIRB use
- Review the reporting requirements when using a CIRB
Target Audience: Clinical Research Coordinator, Clinical Research Nurse, Data Manager, Manager of Regulatory Affairs, Investigator, Medical Research Scientist, Pharmacist, Project Manager, Quality Control Specialist, Research Manager, Research Technician or Assistant, Statistician, Trainer
Registration Cost: FREE to all Chapter, ACRP, and non-members including lunch
Contact hours: 1.0 ACRP contact hours are available for this presentation.
Membership is not required for online registration of contact hours.
To receive contact hours: Purchase the contact hours, sign in at the registration desk, and attend the program. Log on to the ACRP website then “ACRP Learning Portal” to complete the evaluation no later than 30 days following the event and obtain the online certificate.
Contact Hour Cost:
- $0 Chapter Members
- $15 ACRP Members
- $30 Non-Members
Refund Policy: Not specified
Level: Not specified
Shelley Welch at 304-293-7348
Connie Cerullo at 240-415-6013