Clinical Research Coordinator A-B

Assists in the management of clinical trials under direct supervision by coordinating patient screening, enrollment, data collection, and sample handling. Supports IRB submissions and helps prepare manuscripts, grant proposals, and presentations. Works closely with the Principal Investigator, manager, and study team to address study needs, implement approved changes, and monitor outcomes. Contributes to investigator-initiated, multi-center, and patient-oriented clinical and translational research studies.

Requirements

• Recruitment, screening, consenting, and enrollment of participants for research studies
• Quantitative and qualitative data collection and management in accordance with study protocols
• Maintenance of electronic databases and data quality checks
• Performing chart reviews and eligibility assessments
• Managing study related materials, documentation, and regulatory files in compliance with IRB and human subjects requirements

Benefits

• Health, Life, and Flexible Spending Accounts
• Tuition
• Retirement
• Time Away from Work
• Long-Term Care Insurance
• Wellness and Work-life Resources
• Professional and Personal Development
• University Resources
• Discounts and Special Services
• Flexible Work Hours
• Penn Home Ownership Services
• Adoption Assistance