Senior Clinical Research Coordinator - Complex Protocols

University of Miami; Miami (FL); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Medical benefits

Dental benefits

Tuition remission

Job summary

The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full-Time Clinical Research Coordinator 3 to work at the UHealth campus in Miami, Fl. This role provides leadership in planning, implementing, monitoring, and evaluating multiple clinical research protocols, ensuring study integrity, and mentoring less experienced coordinators.

Responsibilities include coordinating complex protocols, developing SOPs, screening and recruitment, sample handling, and ensuring

Qualifications

• Bachelor’s degree in relevant field required.
• Current Research Coordinator certification by ACRP or SoCRA for minimum 6 months.
• Minimum 4 years of relevant experience.

Responsibilities

• Coordinate implementation of multiple complex clinical research protocols.
• Develop SOPs and templates with guidance from PI/Clinical Research Manager.
• Oversee eligibility screening and study recruitment activities; improve accrual.
• Manage sample processing, packing, and shipping per protocol and regulations.
• Plan and monitor reporting on protocol deviations and unanticipated occurrences.
• Lead protocol implementation and keep investigators informed of progress.
• Organize site visits and auditing activities as assigned.
• Coordinate study visits with data collection schedules and patient progress.

Skills

Learning Agility

Teamwork

Technical Proficiency

Communication

Education

Bachelor’s degree in relevant field

Job description

The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full-Time Clinical Research Coordinator 3 to work at the UHealth campus in Miami, Fl. This role provides leadership in planning, implementing, monitoring, and evaluating multiple clinical research protocols, ensuring study integrity, and mentoring less experienced coordinators.

Responsibilities include coordinating complex protocols, developing SOPs, screening and recruitment, sample handling, and ensuring