Senior Pediatric Clinical Trials Coordinator

University of Florida

Gainesville (FL)

On-site

USD 60,000 - 82,000

Full time

3 days ago
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Job summary

University of Florida in Gainesville seeks a Clinical Research Coordinator III to coordinate clinical studies within the Department of Pediatrics - Child Health Research Institute, focusing on inherited muscular diseases. The role involves independent coordination across the full trial life cycle and collaboration with a multidisciplinary team.

Responsibilities include onboarding new studies, ensuring regulatory compliance, managing study billing, enrolling patients, coordinating visits,

Qualifications

  • Bachelor's degree in an appropriate area; 3 years of relevant experience or equivalent.
  • Experience with clinical trial process and policies.
  • Excellent interpersonal and written/verbal communication skills.
  • Ability to work independently and manage multiple trials.

Responsibilities

  • Onboard new clinical studies following institutional workflows and requirements.
  • Obtain and maintain regulatory compliance.
  • Verify study-related charges following institutional and departmental timelines.
  • Serve as point of contact for all administrative matters related to assigned studies.
  • Enroll patients into assigned clinical studies.
  • Coordinate patient and study monitor site visits.
  • Present study updates at weekly team meetings.
  • Actively participate in the writing of grants, papers, etc.

Skills

Interpersonal skills
Independent work
Problem solving
Decision making
Microsoft Office

Education

Bachelor's degree in an appropriate area

Tools

Microsoft Office

Job description

University of Florida in Gainesville seeks a Clinical Research Coordinator III to coordinate clinical studies within the Department of Pediatrics - Child Health Research Institute, focusing on inherited muscular diseases. The role involves independent coordination across the full trial life cycle and collaboration with a multidisciplinary team.

Responsibilities include onboarding new studies, ensuring regulatory compliance, managing study billing, enrolling patients, coordinating visits,

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