Clinical Research Project Manager, Palliative Care & Equity

Trustees of University of Pennsylvania; Philadelphia (Philadelphia County); On-site; USD 63,000 - 71,000; Full time

Job summary

The Trustees of the University of Pennsylvania’s Perelman School of Medicine seeks two Clinical Project Managers A to support PAIR Center trials. You will work with Principal Investigators and external partners to monitor enrollment, protocol adherence, and data reporting across multiple clinical sites.

You will supervise staff, ensure regulatory compliance, and help with proposal development, study design, and manuscript preparation. Excellent communication is essential."

Qualifications

• Bachelor's degree and 3-5 years of prior experience in complex health services research.
• Demonstrated ability to manage scope, timelines, and budget of a large study.
• Excellent verbal and written communication skills; ability to liaise with multiple stakeholders.

Responsibilities

• Manage implementation of study protocols with investigators and clinical site partners.
• Oversee daily operations of the clinical trials, including enrollment and milestones, and supervise research staff.
• Coordinate with data managers and analysts to develop study databases, reports, and analysis plans.
• Interface with clinical sites to ensure consistency and quality in study implementation.
• Manage regulatory compliance including IRB submissions and progress reports to sponsors.
• Coordinate team and stakeholder meetings; develop manuals of procedures.
• Contribute to proposal development, study design, methods, interpretation of results, and manuscript development.
• Perform other duties as assigned.

Skills

Clinical trials

Communication skills

Education

Bachelor's degree

Job description

The Trustees of the University of Pennsylvania’s Perelman School of Medicine seeks two Clinical Project Managers A to support PAIR Center trials. You will work with Principal Investigators and external partners to monitor enrollment, protocol adherence, and data reporting across multiple clinical sites.

You will supervise staff, ensure regulatory compliance, and help with proposal development, study design, and manuscript preparation. Excellent communication is essential."