Clinical Research Coordinator A

About the role

The University of Pennsylvania is a world-renowned leader in education, research, and innovation. It consistently ranks among the top 10 universities in the annual U.S. News & World Report survey. The university offers a competitive benefits package that includes excellent healthcare and tuition benefits for employees and their families, generous retirement benefits, a wide variety of professional development opportunities, supportive work and family benefits, a wealth of health and wellness programs and resources, and much more.

Job Responsibilities

• Coordinate and conduct clinical studies, including subject recruitment, informed consent, chart maintenance, and data entry
• Coordinate IRB submissions and renewals in accordance with FDA and IRB guidelines
• Affirm compliance with the protocol and regulatory requirements, including collecting, recording, and maintaining data and source documentations
• Oversee study preparation and blood sample processing and analysis
• Database management and analysis
• Ordering and stocking supplies, maintaining equipment
• Education of patients and family members
• Promotion of good clinical practice in the conduct of clinical investigations

Qualifications

• Bachelor of Science and 1 to 2 years of experience or equivalent combination of education and experience is required

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
• Flexible Work Hours
• Penn Home Ownership Services
• Adoption Assistance