Regulatory Submissions Coordinator

Medpace, Inc. is a growing Contract Research Organization (CRO) 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. Some of the responsibilities will include 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 track submissions and ensure timely filing of documents.

For more information about Medpace, please visit our website at www.Medpace.com.
REQUIREMENTS
Candidate must have a BA/BS in Life Sciences with 2 to 4 years in Regulatory Affairs. Hands-on experience preparing and submitting regulatory documentation is preferred.