Clinical Research Coordinator (CRC)
Location: Indianapolis
Duration: 6+ month contract
Schedule: Monday–Friday, ~40 hours/week (some flexibility based on clinic or study needs)
Role Overview
Coordinates both sponsor-initiated and investigator-initiated oncology-focused clinical trials. Responsible for identifying, screening, and enrolling eligible participants; ensuring compliance with study protocols; and serving as the primary liaison between the study team, participants, and sponsors.
Key Responsibilities
Study Coordination & Participant Management
Data Collection & Regulatory Compliance
Team & Sponsor Collaboration
Administrative & Operational Support
Qualifications
Education:
Skills & Abilities:
Additional Notes
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