About this role
CLINICAL RESEARCH OPERATIONS COORDINATOR - FULL TIME at Employer. Location: Maumee, Ohio, United States. Role: coordinating care, managing enrollment, entering data Requirements: Bachelor's required (master's preferred). Certification in Human Subjects Protection and Good Clinical Practices (GCP) within 30 days of hire. Experience in clinical research or medical practice operations, EDC/data entry, Microsoft Office, and oncology terminology. Category: Research and Development (R&D) Seniority: Mid Level Tools: Microsoft Office, Microsoft Word, Internet, Database, Electronic Data Capture (EDC) Certifications: human subjects protection, good clinical practices (gcp) Commitment: Full Time Workplace: Onsite Languages: English