Sr. Clinical Research Coordinator (Health, Behavior and Society)
Core
Oversee day-to-day activities of complex clinical research studies, including participant recruitment, data collection, and regulatory compliance for the Long-Life Family Study.
Role type
Senior Clinical Research Coordinator
Builds
Clinical trials and studies for disease prevention and treatment
Domain
Public health and clinical research
Deliverable
client delivery
Required skills
Clinical trial management, participant recruitment, data collection and reporting, regulatory compliance, study budget development, standard operating procedure creation, informed consent processes, site audit coordination, literature search, data abstraction
Preferred skills
Master's degree in a related field
Technologies
Clinical Trial Management System
Responsibilities
Develop standard operating procedures and data collection forms from protocols; Prepare materials for submission to IRB; Develop and oversee implementation of recruitment strategies; Set up and ensure validity of data collection systems; Organize and quality control study data; Perform self-audits and audit other sites; Coordinate travel logistics for research assistants; Track and monitor biospecimen deliveries and data uploads
Seniority
Senior, hands-on IC