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.

Requirements

• recruitment, screening, consenting, and enrollment of participants for research studies
• quantitative and qualitative data collection and management in accordance with study protocols
• performing chart reviews and eligibility assessments
• managing study related materials, documentation, and regulatory files
• communicating with study participants

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
• Discounts and Special Services
• Flexible Work Hours
• Penn Home Ownership Services
• Adoption Assistance