Clinical Research Coordinator 2

About the role

The University of Miami’s UHealth campus is seeking a full‑time Clinical Research Coordinator 2 to support the planning, execution, and oversight of moderate‑risk clinical studies. This mid‑level position will manage day‑to‑day protocol activities from initiation through close‑out while 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 for clinical protocols.
• Process, pack, and ship biological specimens in accordance with protocol and regulatory standards.
• Maintain study documentation, binders, and filing systems per university and sponsor requirements.
• Distribute study drug materials under the Principal Investigator’s delegation.
• Monitor, document, and report adverse events and protocol deviations.
• Support implementation of protocol amendments and conduct study orientation sessions.
• Track study progress, prepare progress reports, and communicate updates to investigators and sponsors.
• Coordinate administrative tasks for study personnel, including training documentation and performance reviews.
• Apply cultural competency practices to meet participants’ language and health‑literacy needs.

Required profile

• Mid‑level clinical research professional with experience in protocol implementation.
• Familiarity with federal, state, and sponsor regulatory guidelines.
• Ability to manage multiple study activities and maintain accurate documentation.
• Strong communication skills for interaction with investigators, sponsors, and study staff.
• Commitment to participant safety and ethical research conduct.

Required skills