Entry-Level Clinical Research Coordinator | REDCap & Data

University of Miami

Miami (FL)

On-site

USD 55,000 - 75,000

Full time

3 days ago
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Job summary

The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full-Time Clinical Research Coordinator 1 to work at UHealth in Miami, Florida.

The Clinical Research Coordinator 1 serves as an entry-level clinical research professional that has a foundation in clinical research through assigned responsibilities in data management or implementing clinical research protocols. The incumbent is responsible for simple clinical research protocols and timelines.

Qualifications

  • Bachelor's degree in relevant field required.
  • Minimum 1 year of relevant experience required.
  • Learning agility, teamwork, technical proficiency, and communication are essential.

Responsibilities

  • Performs chart review/pre-screening for eligibility and coordinates simple protocols.
  • Coordinates routine data collection, visits, scheduling, and study progress.
  • Performs moderate to complex research tests and adapts procedures under supervision.
  • Operates clinical research equipment per instructions and troubleshoots issues.
  • Observes and reports adverse events and ensures participant safety per protocol.
  • Manages regulatory documentation and adheres to institutional and regulatory requirements.
  • Maintains study records, REDCap data, and communications with participants and sites.
  • Travels to Sylvester clinics and partner sites to identify and recruit participants.

Skills

Learning Agility
Teamwork
Technical Proficiency
Communication

Education

Bachelor's degree

Job description

The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full-Time Clinical Research Coordinator 1 to work at UHealth in Miami, Florida.

The Clinical Research Coordinator 1 serves as an entry-level clinical research professional that has a foundation in clinical research through assigned responsibilities in data management or implementing clinical research protocols. The incumbent is responsible for simple clinical research protocols and timelines.

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