About this role
Clinical Research Regulatory Coordinator at Employer. Location: Cortland or Horseheads. Role: preparing submissions, managing regulatory, conducting reviews Requirements: 2+ years clinical research regulatory experience, Associate's degree, IRB submission and regulatory maintenance experience, REALTIME and Microsoft Office proficiency, knowledge of ICH-GCP and FDA regulations. Category: Research and Development (R&D) Seniority: Entry Level Tools: REALTIME CTMS, REALTIME, Microsoft Office Commitment: Full Time Workplace: Onsite Languages: English