Assists with the administrative components required to ensure compliance in the regulatory processes for a clinical research project. This role involves creating and maintaining study binders, preparing and submitting IRB documents, ensuring accuracy and congruency between various regulatory and financial systems, and managing document retrieval and archival processes at study termination. The coordinator will also work with marketing and research staff to ensure studies utilizing recruitment tactics are posted appropriately.
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Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree