Clinical Trials Coordinator I: Start-Up & Compliance

University of Central Florida - College of Medicine

Orlando (FL)

On-site

USD 56,000 - 69,000

Full time

2 days ago
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Benefits offered by this job

Medical, Dental, Vision, Life
Paid time off
Retirement savings options
Employee discounts
Education assistance

Job summary

The University of Central Florida College of Medicine is seeking an experienced Clinical Research Coordinator I to support the Manager-Clinical Trials with business development, regulatory submissions, study activation, and ongoing trial operations. The role involves coordinating with sponsors, monitors, auditors, and research staff to ensure timely activation and compliant study conduct.

Responsibilities include budgeting, vendor interactions, consent sessions, data entry, and participating in

Qualifications

  • Bachelor's or Master's degree and 2+ years of relevant experience.
  • Pursuant to Fla. Stat. 112.219(6).
  • Experience with data management.
  • Experience with patient care.

Responsibilities

  • Assist with business development by building rapport with industry sponsors, grantors and funders.
  • Navigate start-up and close-out processes for clinical research projects and trials.
  • Prepare regulatory submissions (IRB, central IRB, FDA) and ClinicalTrials.gov applications.
  • Coordinate study activities including consent sessions, data entry, and scheduling.
  • Monitor quality, ensure protocol compliance, and support audits/monitors.
  • Serve as project manager for short-term business-related projects.

Job description

The University of Central Florida College of Medicine is seeking an experienced Clinical Research Coordinator I to support the Manager-Clinical Trials with business development, regulatory submissions, study activation, and ongoing trial operations. The role involves coordinating with sponsors, monitors, auditors, and research staff to ensure timely activation and compliant study conduct.

Responsibilities include budgeting, vendor interactions, consent sessions, data entry, and participating in

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