Part-Time Clinical Research & Data Coordinator

University of Miami; Coral Gables (FL); On-site; USD 42,000 - 60,000; Part time

Job summary

University of Miami seeks a Research Support Coordinator to collect, compile, document, and analyze clinical and genetic research data across multiple studies. You will coordinate professional development with the project team and serve as liaison with partners.

Responsibilities include participant recruitment, consent, IRB document support, data quality assurance, and manuscript preparation. This role emphasizes collaboration, strong communication, and rigorous data handling in a dynamic

Qualifications

• Bachelor’s degree in relevant field required.
• Minimum 2 years of relevant experience required.
• Certification requirements as specified by department.

Responsibilities

• Organizes, hosts, and participates in community education outreach activities to recruit study participants.
• Serves as the primary contact person for referral sites.
• Meets with study participants to explain the purpose of the study and study procedures and obtains informed consent.
• Assists with the preparation and monitoring of IRB documents, administers clinical interviews, and coordinates all assessment and patient contact activity.
• Tracks participants through all stages of the research program.
• Ensures that relevant protocols are implemented in a rigorous fashion and supervises the implementation of data quality assurance procedures.
• Handles petty cash for study activities and organizes data forms.
• Participates in manuscript, report, and grant proposal preparation.
• Monitors revenue cycle for external contracts and relationships, including functions outsourced, core and bolt-on technologies, specialty recovery vendors, and collection agencies.
• Adheres to University and unit-level policies and procedures and safeguards University assets.

Skills

Learning Agility

Teamwork

Technical Proficiency

Communication

Education

Bachelor's degree

Job description

University of Miami seeks a Research Support Coordinator to collect, compile, document, and analyze clinical and genetic research data across multiple studies. You will coordinate professional development with the project team and serve as liaison with partners.

Responsibilities include participant recruitment, consent, IRB document support, data quality assurance, and manuscript preparation. This role emphasizes collaboration, strong communication, and rigorous data handling in a dynamic