Clinical Research Coordinator
Posted Updated
- Location: Appleton, WI
- Facility: St. Elizabeth Hospital
- Department/Specialty: Oncology Research
- Schedule: Day Shift l Full-time
- Collaborate with primary investigator, sponsor and research staff to plan, conduct and evaluate project protocols. Monitor and report on progress of projects.
- Assist with the recruitment, selection, scheduling, and monitoring of research project participants. Manage the handling of adverse events, compliance and other participant-related issues.
- Coordinate the preparation and delivery of departmental communications, presentations and marketing/educational materials.
- Collaborate to ensure compliance with applicable regulations and standards. Assist with responding to and preparing for audits.
- Coordinate activities for the Institutional Review Board (IRB).
- Prepare and maintains documents, presentations, files, training materials and databases needed for IRB compliance.
Licensure / Certification / Registration:
- Certification specializing in Research Professional preferred.
- Research Professional preferred.
Education:
- High School diploma equivalency with 2 years of cumulative experience OR Associate's degree/Technical degree OR 4 years of applicable cumulative job specific experience required.