Research Program Coordinator (Center for Psychedelic & Consciousness Research)
Core
Oversee day-to-day activities of clinical research projects including recruitment, screening, and data collection under the direction of the Principal Investigator.
Role type
Clinical research program coordinator
Builds
Clinical trials and studies to discover new ways to prevent and treat diseases
Domain
Healthcare / Clinical Research
Required skills
Clinical trial management, Data collection, Regulatory compliance, Participant recruitment, Data entry, Protocol implementation, Budget management, IRB liaison
Preferred skills
Human subjects research experience, Master's degree in related field
Technologies
Clinical Trial Management System
Responsibilities
Coordinate all activities of a clinical research study to ensure adherence to protocol, Conduct the consenting process, Schedule participants for required activities, Enter and organize data, Assist with preparation of submissions to the Institutional Review Board (IRB), Oversee budget expenditures for study operations
Seniority
Mid-level, hands-on coordinator