Clinical Research Coordinator 2 – Full Time

About the role

The University of Miami’s Bascom Palmer Eye Institute is seeking a full‑time Clinical Research Coordinator 2 to support the planning, execution, and oversight of moderate‑risk clinical studies. This mid‑level professional will manage day‑to‑day protocol activities from initiation through close‑out, ensuring participant safety and regulatory compliance.

Key responsibilities

• Assist with recruitment, screening, and retention of study participants.
• Perform study procedures, collect data, and manage routine tests.
• Process, pack, and ship biological specimens according to protocol and regulations.
• Maintain study binders, filings, and documentation in line with university and department policies.
• Distribute study drug materials under the Principal Investigator’s delegation.
• Monitor, document, and report adverse events and protocol deviations.
• Support protocol amendments, orientation sessions, and in‑service training.
• Track study progress, prepare progress reports, and keep investigators informed.
• Facilitate communication with sponsors, data coordinating centers, compliance monitors, and collaborating investigators.
• Handle administrative tasks such as orientation, competency documentation, and performance reviews.

Required profile

• Mid‑level clinical research experience with a solid understanding of regulatory and sponsor guidelines.
• Ability to work collaboratively with multidisciplinary teams and external partners.
• Strong organizational skills to manage multiple study activities simultaneously.
• Commitment to cultural competency, including language translation and health‑literacy considerations.

Required skills

What we offer

• Opportunity to work at a world‑renowned eye institute.
• Engagement in cutting‑edge clinical research projects.
• Professional development and training opportunities.