FULL TIME (M-F)

Description:

A Regulatory Coordinator is a vital part of the cancer research team. They are responsible for making sure our clinical trials program stays in compliance with Good Clinical Practice (GCP), the U.S. Food and Drug Administration (FDA), and the Code of Federal Regulations (CFR).

They are involved with the research program making sure each staff delegated authority on a trial is documented and trained or holds a license allowing their participation.

They work closely with Pharmaceutical companies, Contract Research Organizations (CROs), and Institutional Review Boards (IRBs) to ensure each clinical trial is safe, ethical and being conducted as intended by the approved protocol.

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Education, Experience, and Personality:

College Degree and/or 2-3 Years of Administrative Assistant and/or Research Experience

This Career Requires Exceptional Organizational Skills and Attention to Detail.

PC & Microsoft Office Skills

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