Job Summary
A company is looking for a Regulatory Coordinator - GI Oncology.
Key Responsibilities
- Prepare and submit all protocol applications, amendments, and informed consent documents for review and approval
- Track and manage assigned new protocol start-up packets and ensure all start-up activities are completed
- Establish and maintain communication with study teams and regulatory agencies to ensure required information is relayed
Required Qualifications
- Bachelor's Degree required
- Experience in a medical or scientific research setting preferred
- Fundamental knowledge of clinical trial conduct preferred
- Knowledge of ICH/GCP, FDA policies, and the IRB submission process
- Proficiency in Microsoft applications and databases required
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