Regulatory Submissions Coordinator
- Job ID:
- Date:09/23/2008
- Location:Cincinnati
- State:Ohio
- Salary:Not Specified Why?
- Job Types:
-
REGULATORY AFFAIRS
Job Description
Position Type: Full-time
Medpace is a global contract research organization (CRO), based in Cincinnati, OH, that manages the clinical trial process for pharmaceutical and biotechnology companies. We are currently seeking a Regulatory Submissions Coordinator to join our Regulatory Affairs team.
Job Duties:
Preparing, reviewing, and filing clinical trial applications and marketing applications to the international health agencies;
Ensuring submissions comply with applicable regulations and guidance documents;
Advising clients on changing regulations and compliance requirements; and
Tracking submissions and ensure timely filing of documents.
Qualifications:
Bachelor’s degree in Life Sciences or a related field;
2-4 years of experience in regulatory affairs; and
Hands-on experience preparing and submitting regulatory documents is preferred.
Travel: None
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