About this role
Clinical Study Coordinator at PSI CRO. Location: Cleveland or Athens or Chattanooga. Role: coordinating studies, entering data, assisting sites Requirements: 2+ years coordinating clinical research studies (or equivalent on-the-job training), GCP, IATA, and CPR required; phlebotomy and clinical research certification (ACRP/SOCRA) preferred; EDC data entry and site support experience. Category: Research and Development (R&D) Seniority: Entry Level Tools: EDC systems Certifications: gcp, iata, cpr, phlebotomy, acrp, socra Commitment: Full Time Workplace: Onsite Languages: English