Clinical Research Coordinator II — Genitourinary Trials

University of Miami

United States

On-site

USD 60,000 - 85,000

Full time

3 days ago
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Job summary

University of Miami is seeking a Clinical Research Coordinator 2 to support the planning, coordination, implementation, and evaluation of clinical studies. This role ensures participant safety and adherence to approved protocols, coordinating study activities across teams and sites.

The candidate will assist in recruitment, perform routine study procedures and data collection, and help maintain regulatory compliance while liaising with sponsors and coordinators to ensure smooth study progress.

Qualifications

  • Bachelor’s degree in relevant field is required.
  • Minimum 2 years of relevant experience is required.
  • Knowledge, Skills and Abilities: strong communication, teamwork, and adaptability.

Responsibilities

  • Assist in participant recruitment and retention activities.
  • Perform study procedures, data collection, and daily operations of moderate risk protocols.
  • Collect, process, pack, and ship specimens per protocol and standards.
  • Maintain study binders and filings per protocol requirements and department policy.
  • Distribute study materials according to clinical credentials and PI guidance.
  • Monitor, document, report, and follow up on adverse events and protocol deviations.
  • Assist with protocol amendments under PI supervision.
  • Support study orientation and in-services for research team.

Skills

Learning Agility
Teamwork
Technical Proficiency
Communication

Education

Bachelor’s degree in relevant field

Job description

University of Miami is seeking a Clinical Research Coordinator 2 to support the planning, coordination, implementation, and evaluation of clinical studies. This role ensures participant safety and adherence to approved protocols, coordinating study activities across teams and sites.

The candidate will assist in recruitment, perform routine study procedures and data collection, and help maintain regulatory compliance while liaising with sponsors and coordinators to ensure smooth study progress.

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