Clinical Research Coordinator (The Institute for Clinical and Translational Research)
Core
Administratively coordinate clinical protocol implementation and provide logistical support for clinical research studies to discover new ways to prevent and treat diseases.
Role type
Clinical Research Coordinator
Builds
Clinical research studies
Domain
Healthcare / Clinical Research
Required skills
Protocol adherence, Participant recruitment, Informed consent, Data entry, IRB submissions, Budget management, Study coordination, Regulatory compliance
Preferred skills
Human subjects research experience
Technologies
Clinical Trial Management System
Responsibilities
Coordinate all activities of a clinical research study to ensure adherence to protocol; Assist research nurses and principal investigators in executing protocol-related activities; Conduct the consenting process; Schedule participants for required activities; Assist with setup of the data collection system and enter data; Assist with the preparation of submissions to the Institutional Review Board (IRB); Oversee budget expenditures for study operations.
Seniority
Mid-level, hands-on IC