Clinical Research Coordinator 2 (a)

University of Miami

Miami, FL, United States
On-site
Study participant recruitment and retention
Perform study procedures and data collection
Process and ship specimens
The University of Miami is seeking a Clinical Research Coordinator 2 who will assist in planning, coordinating, and implementing various clinical research studies within the Surgery department. This role requires a Bachelor's degree and at least two years of relevant experience, with responsibilities including participant recruitment, data collection, and adherence to study protocols

Job Summary

  • The incumbent serves as a mid-level clinical research professional that assists in the planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies.
  • This role assists in the day-to-day operations of clinical research protocol implementation and carries out study coordination duties from protocol initiation to study close-out according to regulatory/sponsor guidelines.
  • The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more.

Matching Summary

Match Score: 85

The University of Miami is seeking a Clinical Research Coordinator 2 who will assist in planning, coordinating, and implementing various clinical research studies within the Surgery department. This role requires a Bachelor's degree and at least two years of relevant experience, with responsibilities including participant recruitment, data collection, and adherence to study protocols.

Skills & Requirements

Must-have

  • Study participant recruitment and retention
  • Perform study procedures and data collection
  • Process and ship specimens
  • Maintain study binders and filings
  • Monitor and report adverse events
  • Adhere to regulatory guidelines

Nice-to-have

  • Facilitate cross-functional communication
  • Assist with study personnel administration
  • Cultural competency and patient needs

Key Requirements

  • Bachelor's degree in relevant field
  • Minimum 2 years of relevant experience
  • Administer informed consent forms
  • Schedule research visits and follow-up
  • Complete patient data forms and review charts

Work Rights

Not specified

Tailored Resume

Cover Letter