Job Summary
A company is looking for a Research Regulatory Coordinator.
Key Responsibilities
- Prepares and submits regulatory documents for Institutional Review Board (IRB) and manages compliance with regulatory agencies
- Organizes and maintains regulatory study documentation and ensures adherence to sponsor and regulatory requirements
- Conducts administrative activities to support clinical trials, including financial tracking and communication facilitation among study teams
Required Qualifications
- Minimum of 3 years of experience in supporting regulatory activities in clinical research
- Associate degree required; Bachelor's degree preferred
- Mandatory education on Human Subject and Good Clinical Practice
- Able to function independently with strong organizational skills
- Excellent communication and interpersonal skills
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