About this role
Clinical Research Coordinator I at Cooper University Hospital. Location: Camden, New Jersey, United States. Role: assisting PI, maintaining documents, recruiting participants Requirements: Prepare IRB protocols and consent forms, maintain study documents, assist with participant identification and recruitment; high school diploma required; research or clinical experience preferred. Category: Research and Development (R&D) Seniority: Entry Level Tools: Microsoft Excel, Microsoft Outlook, Microsoft Word Commitment: Full Time Workplace: Onsite Languages: English