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!

Job Tags

Contract work, Local area,

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