Clinical Research Coordinator-256930
Medix™
We are seeking a detail-oriented Clinical Research Coordinator with proven CRIO eSource experience and hands-on clinical skills to oversee participant visits and trial compliance. Key Responsibilities Trial Coordination: Schedule and coordinate participant visits, study procedures, and day-to-day workflow. Data & eSource: Manage source documentation and data entry within CRIO eSource/eCTMS. Compliance & Regulatory: Ensure strict protocol compliance, maintain regulatory documents, and keep study records audit-ready. Team Collaboration: Partner with sponsors, principal investigators, and site personnel to ensure data accuracy and patient safety. Required Qualifications 2–3+ years of direct Clinical Research Coordinator (CRC) experience. Independent CRIO Proficiency: Demonstrated experience using CRIO eSource/eCTMS (must be able to navigate the system independently). Hands-on Clinical Skills: Demonstrated experience in phlebotomy and administering injections. #J-18808-Ljbffr Medix™
Vacancy posted 2 days ago
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