Job Summary

• Senior Clinical Research Coordinator serves as lead resource in the execution of assigned clinical research studies in accordance with approved protocols administered by the Clinical Trials Office (CTO) Multi-Center Trial Program (MCTP).
• Oversees & coordinates conduct of daily activities of research studies; serves as primary reviewer of subsite patient records to assess and identify patients who meet criteria for participation in research studies.
• Assists with activities to ensure compliance with Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations; participates in planning, organizing and preparing for external compliance and quality assurance and control reviews.

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Skills & Requirements

Key Requirements

• Bachelor’s Degree in biological sciences, health sciences or medical field or equivalent
• three to five years experience in clinical research
• clinical research certification required
• computer skills required

Work Rights