About this role
Coordinator - Clinical Research I - FT - Days - OHR at Memorialhealthcare. Location: United States. Role: coordinating studies, managing compliance, processing specimens Requirements: Coordinates clinical research studies, manages adverse events and compliance, prepares IRB submissions, supports monitoring and audits. High school diploma required. No prior experience required. Category: Research and Development (R&D) Seniority: No Prior Experience Required Commitment: Full Time Workplace: Onsite Languages: English