Research Program Coordinator (Center for Psychedelic and Consciousness Research)
Core
Coordinate clinical research studies, manage participant recruitment and consent, and oversee laboratory specimen processing for the Center for Psychedelic and Consciousness Research.
Role type
Clinical Program Coordinator
Builds
Clinical research studies and data collection systems
Domain
Biomedical research / Clinical trials
Required skills
Clinical trial coordination, Participant recruitment, Informed consent administration, Data entry, Laboratory specimen processing, Phlebotomy, Regulatory compliance, Budget management
Preferred skills
Human subjects research experience, Phlebotomy certification
Technologies
Clinical Trial Management System, Laboratory computer systems
Responsibilities
Coordinate study activities to ensure protocol adherence, Conduct participant recruitment and screening, Administer informed consent, Process blood and saliva specimens, Maintain specimen inventory and ship frozen materials, Assist with data collection and system setup, Liaise with IRB and study personnel, Oversee study budget expenditures