Clinical Research Coordinator II: End-to-End Trial Support

University of Miami; Miami (FL); On-site; USD 60,000 - 85,000; Full time

Benefits offered by this job

Competitive salary

Comprehensive benefits

Tuition remission

Job summary

The University of Miami is seeking a Clinical Research Coordinator 2 to support planning, coordinating, implementing, monitoring, and evaluating clinical studies. You will assist in day-to-day protocol operations, ensure participant safety, and maintain regulatory compliance across multiple trials.

The role liaises with study teams, sponsors, and staff to facilitate smooth study progress. Responsibilities include recruitment activities, performing study procedures, specimen handling, data entry

Qualifications

• Bachelor’s degree in a relevant field is required.
• Minimum 2 years of relevant experience is required.
• Ability to learn procedures, adapt to changing priorities, and work in a team.

Responsibilities

• Assist in participant recruitment and screening for eligibility.
• Perform study procedures, data collection and daily operations for moderate risk protocols.
• Collect, process, pack and ship specimens per protocol and guidelines.
• Maintain study binders and files; support IP handling and accountability.
• Monitor adverse events and protocol deviations; assist with amendments under PI supervision.
• Coordinate startup and ongoing operations including SIVs, monitoring visits, and audits.

Skills

Learning Agility

Teamwork

Technical Proficiency

Communication

Education

Bachelor’s degree in relevant field

Job description

The University of Miami is seeking a Clinical Research Coordinator 2 to support planning, coordinating, implementing, monitoring, and evaluating clinical studies. You will assist in day-to-day protocol operations, ensure participant safety, and maintain regulatory compliance across multiple trials.

The role liaises with study teams, sponsors, and staff to facilitate smooth study progress. Responsibilities include recruitment activities, performing study procedures, specimen handling, data entry