Job Summary
A company is looking for a Regulatory Coordinator to manage regulatory operations for clinical research protocols.
Key Responsibilities
- Oversee day-to-day regulatory operations and manage the regulatory team's workload
- Provide regulatory support for research programs and maintain required regulatory documents
- Coordinate timely regulatory submissions and assist with standard regulatory-related training
Required Qualifications
- Bachelor's degree in Clinical Health Science or Healthcare Administration
- 2 years of Clinical Research Experience preferred
- Proficient in computer usage and Microsoft software
- Experience with electronic health record systems and clinical trial management systems preferred
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