University of Miami
Clinical Research Coordinator 2 - University of Miami
Full‑time position located at the UHealth campus in Miami, FL. Internal applicants may use the University of Miami Workday system to apply. If you are a current staff, faculty or temporary employee, click the link to log in to Workday. Core Job Summary
The Clinical Research Coordinator 2 serves as a mid‑level clinical research professional that assists in the planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies. The role supports day‑to‑day operations of protocol implementation, coordinating study activity from initiation through close‑out in compliance with regulatory and sponsor guidelines. Core Job Functions (Responsibilities)
Assist in participant recruitment, retention, and screening for eligibility. Perform study procedures, routine tests, and data collection/recording for moderate‑risk protocols. Collect, process, pack, and ship specimens according to protocol and regulatory standards. Maintain study binders and filings per protocol, University, and department policy. Distribute study drug materials per practice standards and delegate instructions from the Principal Investigator. Monitor and document study unanticipated/adverse events and protocol deviations; follow up and report accordingly. Assist in implementing protocol amendments under supervision of the Principal Investigator. Provide study orientation and protocol‑related in‑services to the research team and clinical staff. Monitor protocol implementation, track study progress, keep investigators informed, and submit progress reports on schedule. Communicate with sponsors, data coordinating centers, compliance monitors, collaborators, investigators, and administrative personnel. Assist with orientation, competency documentation, safety education, and performance reviews for study personnel. Adhere to cultural competency guidelines and implement strategies for language translation and health literacy. Follow all international, national, and local regulatory requirements. Maintain mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies. Adhere to University and unit‑level policies to safeguard University assets. Core Qualifications
Education: Bachelor’s degree in a relevant field. Experience: Minimum 2 years of relevant experience. Knowledge, Skills and Attitudes: Accurate assignment completion with attention to detail. Analytical, organized, and ability to prioritize work under pressure, meeting deadlines. Confidential information handling with discretion. Availability to work evenings, nights, and weekends as necessary. Commitment to the University’s core values. Ability to work independently and in a collaborative environment. Benefits
The University of Miami offers competitive salaries and a comprehensive benefits package, including medical, dental, tuition remission, and more. UHealth – University of Miami Health System is South Florida’s only university‑based health system. We provide leading‑edge patient care powered by groundbreaking research and education at the Miller School of Medicine. Our faculty represent over 100 specialties, handling more than one million patient encounters each year. Equal Opportunity
The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by federal law. Job Details
Job Status: Full time. Employee Type: Staff.
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Full‑time position located at the UHealth campus in Miami, FL. Internal applicants may use the University of Miami Workday system to apply. If you are a current staff, faculty or temporary employee, click the link to log in to Workday. Core Job Summary
The Clinical Research Coordinator 2 serves as a mid‑level clinical research professional that assists in the planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies. The role supports day‑to‑day operations of protocol implementation, coordinating study activity from initiation through close‑out in compliance with regulatory and sponsor guidelines. Core Job Functions (Responsibilities)
Assist in participant recruitment, retention, and screening for eligibility. Perform study procedures, routine tests, and data collection/recording for moderate‑risk protocols. Collect, process, pack, and ship specimens according to protocol and regulatory standards. Maintain study binders and filings per protocol, University, and department policy. Distribute study drug materials per practice standards and delegate instructions from the Principal Investigator. Monitor and document study unanticipated/adverse events and protocol deviations; follow up and report accordingly. Assist in implementing protocol amendments under supervision of the Principal Investigator. Provide study orientation and protocol‑related in‑services to the research team and clinical staff. Monitor protocol implementation, track study progress, keep investigators informed, and submit progress reports on schedule. Communicate with sponsors, data coordinating centers, compliance monitors, collaborators, investigators, and administrative personnel. Assist with orientation, competency documentation, safety education, and performance reviews for study personnel. Adhere to cultural competency guidelines and implement strategies for language translation and health literacy. Follow all international, national, and local regulatory requirements. Maintain mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies. Adhere to University and unit‑level policies to safeguard University assets. Core Qualifications
Education: Bachelor’s degree in a relevant field. Experience: Minimum 2 years of relevant experience. Knowledge, Skills and Attitudes: Accurate assignment completion with attention to detail. Analytical, organized, and ability to prioritize work under pressure, meeting deadlines. Confidential information handling with discretion. Availability to work evenings, nights, and weekends as necessary. Commitment to the University’s core values. Ability to work independently and in a collaborative environment. Benefits
The University of Miami offers competitive salaries and a comprehensive benefits package, including medical, dental, tuition remission, and more. UHealth – University of Miami Health System is South Florida’s only university‑based health system. We provide leading‑edge patient care powered by groundbreaking research and education at the Miller School of Medicine. Our faculty represent over 100 specialties, handling more than one million patient encounters each year. Equal Opportunity
The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by federal law. Job Details
Job Status: Full time. Employee Type: Staff.
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