Job Summary
A company is looking for a Regulatory Coordinator - Breast Oncology.
Key Responsibilities
- Prepare and submit protocol applications, amendments, and regulatory documents for review and approval
- Track and manage new protocol start-up packets, ensuring all activities are completed on time
- Maintain communication with study teams and regulatory agencies to ensure compliance and documentation
Required Qualifications and Education
- Bachelor's Degree required
- Experience in a medical or scientific research setting preferred
- Fundamental knowledge of clinical trial conduct preferred
- Understanding of regulatory policies and IRB submission processes
- Proficiency in Microsoft applications and databases
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