University of Florida
Study Coordinator I
🇺🇸 Gainesville, FL
🕑 Full-Time
💰 $48K - $55K
💻 Operations
🗓️ July 15th, 2025
Edtech.com's Summary
- Coordinate care and protocol-required testing for subjects enrolled in human clinical trials.
- Interpret and collect medical and clinical data for trial subjects.
- Maintain compliance with internal and external regulatory and institutional requirements.
- Manage sample collection, analysis, and shipping for clinical trials.
- Compensation ranges from $48,000 to $55,000 annually with benefits including health insurance, retirement plans, paid leave, tuition assistance, and loan forgiveness eligibility.
- Requires an Associate’s degree or allied health professional degree with one year of relevant experience or equivalent combination; clinical research certification through SOCRA or ACRP within 12 months of hire is mandatory.
- Preferred qualifications include a Bachelor’s degree in health care or basic sciences, relevant research or oncology experience, and proficiency with Microsoft Office (Outlook, Excel, Word).
- Must demonstrate strong interpersonal skills, emotional intelligence, confidentiality, effective communication, project management, and ability to handle competing demands.
- Work collaboratively with investigators, physicians, clinical staff, sponsors, and external partners across a multidisciplinary cancer center.
- Entry-level role ideal for launching a clinical research career in a prominent NCI-designated cancer center.
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