Clinical Research Coordinator I
$52,666–$84,282 year
On-site · St. Petersburg, Florida, United States
Job Summary
Coordinate assigned oncology clinical research studies as a CRC I within the Pediatric Oncology Research Program. Serve as liaison between study teams, sponsors, hospital departments, and the IRB; recruit, screen, consent, and follow participants per protocol; prepare/regulatory submissions to sponsors and IRBs; coordinate study visits, interventions, and data collection; monitor and report adverse events and protocol deviations; enter study data into research databases and maintain audit-ready regulatory binders and participant records.
Required Qualifications
- Bachelor’s degree in a science, health-related, or similar field
- Minimum of 2 years of experience in clinical research, direct patient care, nursing, or another healthcare-related role
- Experience using Electronic Medical Records (EMR)
- Proficiency with Microsoft Office (Word, Excel, Outlook)
- Strong communication, organizational, and time-management skills
- Ability to follow research protocols and regulatory requirements closely
Desired Qualifications
- Clinical research experience in oncology preferred
- Familiarity with Good Clinical Practice (GCP), FDA regulations, and IRB processes (preferred)
- Experience with REDCap, OnCore, Rave, Veeva Vault, or similar research systems (preferred)
- Clinical research certification (CCRC, CCRP, or equivalent) (preferred)
Apply with one swipe on Sorce. We auto-fill applications and apply on your behalf — no cover letters, no 40-minute forms.
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.