University of Miami
Overview
The University of Miami Health System is hiring a full‑time Clinical Research Coordinator 2 to support the planning, coordination, and monitoring of clinical research studies at the UHealth medical campus in Miami, FL. The role assists in protocol implementation, participant recruitment, data collection, and study close‑out activities while ensuring regulatory and sponsor compliance. Responsibilities
Assist in participant recruitment, screening, and retention activities. Perform study procedures, routine tests, and daily operations for moderate risk clinical research protocols. Collect, process, pack, and ship specimens according to protocol standards. Maintain study binders, filings, and drug distribution in accordance with protocol and university policy. Monitor, document, and report unanticipated adverse events, protocol deviations, and study progress. Assist in study protocol amendments, orientation, and in‑service training for the research team. Coordinate communication with sponsor, data coordinating centers, and regulatory compliance monitors. Adhere to university and unit‑level policies, safeguarding university assets. Qualifications
Bachelor’s degree in a relevant field (minimum 2 years of relevant experience). Skill in completing assignments accurately with attention to detail. Ability to analyze, organize, and prioritize work under pressure while meeting deadlines. Discretion in handling confidential information. Availability to work evenings, nights, and weekends as necessary. Commitment to the University’s core values and ability to work independently or collaboratively. Benefits
Competitive salary range: $50,000.00 – $100,000.00. Full benefits package including medical, dental, tuition remission, and more. The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on categories protected by Federal law.
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The University of Miami Health System is hiring a full‑time Clinical Research Coordinator 2 to support the planning, coordination, and monitoring of clinical research studies at the UHealth medical campus in Miami, FL. The role assists in protocol implementation, participant recruitment, data collection, and study close‑out activities while ensuring regulatory and sponsor compliance. Responsibilities
Assist in participant recruitment, screening, and retention activities. Perform study procedures, routine tests, and daily operations for moderate risk clinical research protocols. Collect, process, pack, and ship specimens according to protocol standards. Maintain study binders, filings, and drug distribution in accordance with protocol and university policy. Monitor, document, and report unanticipated adverse events, protocol deviations, and study progress. Assist in study protocol amendments, orientation, and in‑service training for the research team. Coordinate communication with sponsor, data coordinating centers, and regulatory compliance monitors. Adhere to university and unit‑level policies, safeguarding university assets. Qualifications
Bachelor’s degree in a relevant field (minimum 2 years of relevant experience). Skill in completing assignments accurately with attention to detail. Ability to analyze, organize, and prioritize work under pressure while meeting deadlines. Discretion in handling confidential information. Availability to work evenings, nights, and weekends as necessary. Commitment to the University’s core values and ability to work independently or collaboratively. Benefits
Competitive salary range: $50,000.00 – $100,000.00. Full benefits package including medical, dental, tuition remission, and more. The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on categories protected by Federal law.
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