Senior Clinical Research Program Manager, QA & Monitoring

University of Miami; Miami (FL); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Medical benefits

Tuition remission

Dental benefits

Job summary

University of Miami/UHealth Department of Public Health is seeking a Sr. Project Manager, Research Support in Miami, FL. The role oversees multiple clinical research projects, ensuring alignment with institutional objectives, regulatory compliance, and quality standards.

Responsibilities include planning, reporting, resource allocation, and team leadership to support complex studies and QA processes. A strong background in clinical research operations and collaboration with study staff is

Qualifications

• Bachelor's degree required in a relevant field.
• Minimum 5 years of experience in clinical research.
• Certification in Clinical Research (ACRP/SOCRA) preferred.
• Knowledge of federal regulations governing clinical research.
• Knowledge of QA/QC monitoring practices.
• Ability to direct and evaluate department operations.

Responsibilities

• Oversees multiple projects aligned to institutional objectives.
• Prepares reports on project status and activities.
• Establishes practices, policies, and partnerships for functions.
• Prepares estimates and detailed project plans for all phases.
• Procures resources to meet objectives within timeframe.
• Monitors staff performance and conducts reviews.
• Ensures compliance with policies and procedures.

Skills

Project management

Leadership

Communication

Coordination

Education

Bachelor's degree in relevant field

Master's preferred

Tools

Office software

Job description

University of Miami/UHealth Department of Public Health is seeking a Sr. Project Manager, Research Support in Miami, FL. The role oversees multiple clinical research projects, ensuring alignment with institutional objectives, regulatory compliance, and quality standards.

Responsibilities include planning, reporting, resource allocation, and team leadership to support complex studies and QA processes. A strong background in clinical research operations and collaboration with study staff is