About this role
Clinical Research HRPP Program Specialist at The University of Toledo. Location: Toledo, Ohio, United States. Role: monitoring regulations, educating personnel, training documents Requirements: Bachelor’s in nursing, public health, healthcare, clinical research or related discipline; 4+ years in academic or regulatory setting with clinical research; experience in training personnel; knowledge of FDA/GCP; proficiency with EPIC and MS Office. Category: Research and Development (R&D) Seniority: Mid Level Tools: EPIC, Microsoft Office Commitment: Full Time Workplace: Onsite Languages: English