"Clinical Research Coordinator A/B"

The Clinical Research Coordinator is responsible for oversight, execution, and regulatory compliance of human subject research carried out in the Stroke Division of the Neurology Department.

The CRC will be responsible for the execution of clinical trials, including patient recruitment, data collection and management, and potentially some regulatory responsibilities. The coordinator must be detail oriented and have prior experience with IRB guidelines and policies and human subject research practices and appropriate professional skills in the execution of research protocols. The Clinical Research Coordinator will receive training in multiple research instruments, such as transcranial doppler ultrasound, optical blood flow monitor, and blood pressure monitors. This position will require significant bedside interaction with patients. The coordinator must be able to function autonomously and effectively manage study protocols.

In addition to the duties above, CRC Bs will manage IRB submissions and potentially help orient/train other CRCs.

Position is contingent on continued funding.