Senior Clinical Research Coordinator: Lead Multi-Protocol Studies

University of Miami; Miami (FL); On-site; USD 70,000 - 95,000; Full time

Job summary

The University of Miami/UHealth Department of SCCC is seeking a Full Time Clinical Research Coordinator 3 at the UHealth campus in Miami, FL. The role leads planning, implementation, monitoring, and evaluation of multiple clinical research protocols, mentors junior coordinators, and ensures study integrity and participant safety.

Responsibilities include coordinating complex protocols, developing SOPs, overseeing recruitment and sample handling, and ensuring compliance with regulatory standards

Qualifications

• Bachelor’s degree in a relevant field is required.
• Certification in Clinical Research (ACRP or SoCRA) or the ability to obtain within six months is required.
• Minimum 4 years of relevant clinical research experience.
• Strong data collection, analysis and problem-solving abilities.
• Ability to manage multiple activities under deadlines while maintaining confidentiality and working independently or with a team.

Responsibilities

• Coordinate implementation of multiple complex clinical research protocols.
• Develop SOPs and templates with guidance from PI/CR Manager.
• Oversee eligibility screening and recruitment; implement accrual strategies.
• Manage sample processing, packing and shipping per protocol and regulations.
• Plan and monitor deviations, incident reporting and corrective actions.
• Disseminate information and ensure regulatory/ethics compliance across sites.

Skills

Data collection

Problem solving

Time management

Confidential information handling

Independent / collaborative work

Education

Bachelor’s degree in relevant field

Certification in Clinical Research (ACRP or SoCRA) or ability to obtain within 6 months

Job description

The University of Miami/UHealth Department of SCCC is seeking a Full Time Clinical Research Coordinator 3 at the UHealth campus in Miami, FL. The role leads planning, implementation, monitoring, and evaluation of multiple clinical research protocols, mentors junior coordinators, and ensures study integrity and participant safety.

Responsibilities include coordinating complex protocols, developing SOPs, overseeing recruitment and sample handling, and ensuring compliance with regulatory standards