Clinical Research Coordinator 3 (A)

About the role

The Department of Medicine at the University of Miami seeks a full‑time Clinical Research Coordinator 3 (A) to lead multiple complex clinical research protocols on the UHealth campus. This experienced professional will oversee study operations from initiation through close‑out, ensuring compliance with regulatory and sponsor requirements.

Key responsibilities

• Coordinate implementation of multiple complex clinical research protocols.
• Develop SOPs and templates in collaboration with the PI and Clinical Research Manager.
• Oversee eligibility screening, recruitment, and strategies to increase participant accrual.
• Manage sample processing, packing, and shipping according to protocol and regulations.
• Monitor, document, and address unanticipated occurrences and protocol deviations.
• Lead site visits, internal and external audits, and research team meetings.
• Synchronize study visits, clinical tests, and data collection schedules.
• Prepare information for research reports and peer‑reviewed publications.

Required profile

• Experienced clinical research professional with a track record of managing multiple studies.
• Strong knowledge of regulatory guidelines and ethical standards.
• Ability to mentor less‑experienced coordinators and collaborate with multidisciplinary teams.

Required skills

• Protocol development and implementation.
• Sample handling, processing, and shipping.
• Regulatory compliance and audit preparation.
• Development of SOPs and best‑practice manuals.

What we offer

• Opportunity to lead high‑impact clinical research projects.
• Collaborative environment within a leading academic medical center.
• Professional development and mentorship opportunities.