Senior Research Program Manager, Clinical Trials

University of Miami; United States; On-site; USD 90,000 - 125,000; Full time

Benefits offered by this job

Medical benefits

Dental benefits

Tuition remission

Job summary

The University of Miami seeks a Senior Project Manager, Research Support, to oversee complex clinical research programs in Miami, FL. The role emphasizes aligning projects with institutional objectives and maintaining rigorous compliance and quality standards.

Core responsibilities include leading study teams, preparing status reports, and coordinating with stakeholders to ensure timely, compliant delivery across research initiatives. This is a full-time, on-site position at UHealth facilities.

Qualifications

• Bachelor's degree required; Master's preferred.
• Minimum 5 years of experience in clinical research.
• Professional Certification in Clinical Research (e.g., ACRP, SOCRA) preferred.
• Knowledge of federal regulations and policies governing clinical research.
• Ability to direct, manage, implement, and evaluate department operations.
• Ability to lead, motivate, develop, and train others.

Responsibilities

• Oversees multiple related projects to ensure alignment with institutional objectives.
• Prepares reports regarding project status and activities.
• Establishes practices, policies, and partnerships to effectively carry out functions.
• Prepares estimates and detailed project plans for all phases.
• Monitors staff performance and completes performance reviews.
• Ensures compliance with regulatory requirements and QA/QC processes.
• Coordinates QA monitoring and site management for clinical research studies.

Skills

Project management

Clinical research

Leadership

Regulatory compliance

QA/QC monitoring

Communication

Training & mentoring

Education

Bachelor's degree

Master's degree

Clinical research certification (ACRP/SOCRA)

Job description

The University of Miami seeks a Senior Project Manager, Research Support, to oversee complex clinical research programs in Miami, FL. The role emphasizes aligning projects with institutional objectives and maintaining rigorous compliance and quality standards.

Core responsibilities include leading study teams, preparing status reports, and coordinating with stakeholders to ensure timely, compliant delivery across research initiatives. This is a full-time, on-site position at UHealth facilities.