Clinical Research Coordinator (Stem Cell Institute)

Job location: Miami, FL

Employment Type: Full-time
Posted data: 2020-11-06
Req: R100042500
Current Employees:If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position using the Career worklet, please review this tip sheet.Transforming LivesThe University of Miami is among the top research universities and academic medical centers in the nation, and one of the largest private employers in South Florida.With more than 16,000 faculty and staff, the University strives for excellence, and is driven by a powerful mission to transform and impact the lives of its students, patients, members of the community, and people across the globe.The University is committed to fostering a culture of belonging, where everyone feels valued and has the opportunity to add value. Through values of Diversity, Integrity, Responsibility, Excellence, Compassion, Creativity, and Teamwork (DIRECCT) the U community works together to create an environment driven by purpose, excellence, community, and service.

About This Position

The Interdisciplinary Stem Cell Institute at the University of Miami, Miller School of Medicine, has an exciting career opportunity for a Clinical Research Coordinator. This position coordinates and supports all research activities at the Interdisciplinary Stem Cell Institute (ISCI).

The duties and responsibilities for this position may include, but are not limited to:

• Recruitment and screening of participants, obtain informed consent, and follow participants in accordance with clinical trial protocols.




• Coordinating research activities such as scheduling screening assessments, randomization, study product interventions, and follow up assessments. Coordinate laboratory specimen processing and shipment of biological specimens.




• Maintain and organize study files and enter data into electronic case report forms (eCRFs).




• Maintains compliance with all required training




• Provides effective leadership and oversight to the administrative aspects of research study.




• Provides assistance with IRB processes (e.g., abiding by requirement for reporting safety or study deviations, initiating modifications to study procedures




• Ensures policy compliance of research funds and maintains confidentiality.




• Responsible for ordering and maintaining stock of necessary supplies.

Minimum