University of Florida
Regulatory Coordinator I
🇺🇸 Gainesville, FL
🕑 Full-Time
💰 $18 - $21 per Hour
💻 Other
🗓️ June 26th, 2025
Edtech.com's Summary
- Manage regulatory compliance for clinical trial portfolios, interpreting federal regulations and IRB policies.
- Coordinate protocol submissions and prepare IRB submission packets.
- Review clinical trial documentation with investigators and study teams to ensure accuracy and consistency.
- Entry-level position suitable for candidates with some clinical research experience or coursework in public health or related fields.
- Required qualifications: high school diploma or equivalent plus one year relevant experience, with clinical research certification required within 12 months of hire.
- Preferred qualifications: Bachelor's degree in basic/social sciences or public health and familiarity with clinical trials coordination.
- Technical skills include proficiency in Microsoft Office, project management basics, data management, and understanding of Good Clinical Practice and research ethics.
- Compensation ranges from $18.00 to $21.00 hourly, with eligibility for excellent benefits including health, dental, vision insurance, retirement plans, paid leave, tuition assistance, and public service loan forgiveness.
- Works in collaboration with investigators, study staff, and regulatory agencies within the University of Florida's comprehensive cancer research environment.
- Must obtain professional clinical research certification (SOCRA, ACRP, etc.) within one year.
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