Clinical Research Coordinator (Behavioral Pharmacology Research Unit)
Core
Administratively coordinates clinical protocol implementation and provides logistical support for behavioral pharmacology research studies to discover new ways to prevent and treat diseases.
Role type
Clinical Research Coordinator
Builds
Clinical trials and studies for disease prevention and treatment
Domain
Healthcare / Behavioral Pharmacology
Deliverable
client delivery
Required skills
Clinical protocol implementation, participant recruitment, informed consent administration, data collection and entry, regulatory compliance (IRB), budget management, study meeting coordination, literature search
Preferred skills
Master's degree in a related field
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 or ensure consent is obtained; Schedule participants for required activities; Assist with setup of the data collection system and enter and organize data; Assist with the preparation of submissions to the Institutional Review Board (IRB); Oversee budget expenditures for study operations.
Seniority
Entry-level to Mid-level, hands-on IC