Clinical Research Coordinator II — Trials & Study Operations

University of Miami; Florida; On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Competitive salaries

Tuition remission

Job summary

University of Miami’s Bascom Palmer Eye Institute in Palm Beach Gardens, FL, is seeking a Clinical Research Coordinator 2 for a full-time staff position. The role supports planning, coordinating, and monitoring clinical studies to ensure participant safety and protocol adherence.

The coordinator will assist in participant recruitment, data collection, specimen handling, regulatory filings, and communication with sponsors and investigators, under supervision of the Principal Investigator.

Qualifications

• Bachelor's degree in a relevant field required.
• Minimum 2 years of relevant experience required.
• Strong communication and interpersonal skills required.

Responsibilities

• Assist in participant recruitment and retention activities and screening for eligibility.
• Perform study procedures, routine tests, data collection, and day-to-day operations of moderate risk protocols.
• Collect, process, package, and ship specimens according to protocol and regulations.
• Maintain study binders and regulatory filings per protocol and policies.
• Distribute study materials per approved procedures and delegated authority.
• Monitor, document, and report adverse events and protocol deviations.
• Assist with protocol amendments under supervision of the Principal Investigator.
• Support study orientation and in-services for the research team and clinical staff.
• Monitor study progress and communicate updates to investigators as required.
• Coordinate communications with sponsors, data coordinating centers, and regulatory bodies.
• Contribute to training, competency documentation, and safety education.

Skills

Learning agility

Teamwork

Technical proficiency

Communication

Education

Bachelor's degree

Job description

University of Miami’s Bascom Palmer Eye Institute in Palm Beach Gardens, FL, is seeking a Clinical Research Coordinator 2 for a full-time staff position. The role supports planning, coordinating, and monitoring clinical studies to ensure participant safety and protocol adherence.

The coordinator will assist in participant recruitment, data collection, specimen handling, regulatory filings, and communication with sponsors and investigators, under supervision of the Principal Investigator.