Recruits, schedules and conducts the daily activities of clinical research participants, liaising with investigators and regulatory staff. Attends regular staff meetings; provides training and guidance on regulations and best practices to new coordinators.
Assists with research portfolios for numerous PIs and departments across the College.
Participates in study qualification and study feasibility activities for report to research manager.
Liaises with PI, Sponsor, Research Manager and OCR Research Finance to support all aspects of study activity.
Supports research manager and investigators with timely reporting of study status, enrollment status, study monitoring, and site visits.
Supervises, schedules and directs less experienced research coordinators in conduct of OCR clinical research activities, and processes.
Liaises with Research Manager, PI, Sponsor for timely scheduling and coordination of pre-site and site initiation visits.
Attends regular meetings with Research Manager, PIs, and study team for update reports and process improvement.
Follows departmental and institutional standard operating procedures (SOPs). Participates in quality control reviews of study activities and chart reviews.
Completes data collection, documentation activities and database queries.
Coordinates research protocol procedures and processes, working closely with Research Manager, study team, and OCR Regulatory team on monitoring visit report findings.
Provides cross-coverage on study activities across OCR as needed.
Participates in additional projects as directed by research manager, as a central office within the Office of Research.
Supports COVID clinical trial support as central office.
Provides cross-coverage across OCR clinical research study support as needed.