Job Summary
A company is looking for a Regulatory Assistant to support compliance with research protocols in clinical trials.
Key Responsibilities
- Assist with regulatory functions in support of clinical research activity
- Prepare protocol submissions to Institutional Review Boards (IRBs) and provide updates on submission status
- Assist with data entry and maintain documents in the OnCore electronic database
Required Qualifications
- Bachelor's degree in biological sciences, health sciences, or life sciences, or equivalent experience
- Experience in a clinical research capacity is desired
- Computer skills required, with knowledge of database software applications preferred
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