About this role
Regulatory Coordinator I at Sluhn. Location: Allentown, Pennsylvania, United States. Role: reviewing protocols, submitting protocols, maintaining records Requirements: Review, prepare, and submit clinical trial protocols to the IRB; maintain regulatory documentation; apply ICH/GCP, FDA, HIPAA and IRB policies; process IND safety reports; strong Microsoft Office skills and attention to detail. Category: Research and Development (R&D) Seniority: Entry Level Tools: Microsoft Word, Microsoft Excel, Microsoft Access, Microsoft Outlook Commitment: Full Time Workplace: Onsite Languages: English