Job Description

I’m working with a university, ranked in the top 100 of National Universities, to hire a Clinical Research Coordinator to their drug studies team.

Location: Onsite in Philadelphia, PA

Contract Duration: 3 month contract with high potential to convert

About this role:

• Coordinate recruitment and enrollment of research participants
• Establish and maintain databases of subjects
• Schedule and conduct study visits
• Collect and enter data; register subjects and study visits in OnCore
• Perform Epic research billing review
• Maintain an up to date regulatory binder
• Schedule and attend sponsor visits and prepare and submit IRB paperwork to ensure compliance with IRB regulations.

Experience:

• Bachelor's degree in life science or health professions field and at least three years of directly related clinical research coordinator experience
• Experience with drug studies is nice to have
• Knowledge of FDA, IRB, Pennsylvania and related regulations
• Prior experience with IRB submissions both local and central is nice to have
• Prior Electronic Data Capture (eDC) data entry skills is nice to have
• Strong written and verbal communication skills with the ability to interact with a diverse population of students, faculty, staff, sponsors, and research participants

Interested? Apply now!

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