About this role
Clinical Study Coordinator at PSI CRO. Location: Tulsa, Oklahoma, United States. Role: coordinating studies, entering data, managing recruitment Requirements: 2+ years coordinating clinical research or equivalent on-the-job experience; GCP, IATA, CPR, phlebotomy and clinical research certification preferred; EDC data entry, recruitment, regulatory and monitoring support skills. Category: Research and Development (R&D) Seniority: Entry Level Tools: EDC Certifications: gcp, iata, cpr, phlebotomy, acrp, socra Commitment: Full Time Workplace: Onsite Languages: English