Clinical Research Regulatory Specialist III

Regulatory Specialist III

Job Type: Open-Ended Contract
Must reside in one of the following states:
Alabama, Alaska, Arizona, Arkansas, Colorado, Connecticut, Florida, Georgia,
Illinois, Indiana, Iowa, Kansas, Louisiana, Maryland, Michigan, Minnesota,
Missouri, Montana, Nebraska, New Jersey, New York, North Carolina, Ohio,
Oklahoma, Pennsylvania, South Carolina, Tennessee, Texas, Virginia
Key Responsibilities

+ Support IND/IDE and biologics submissions, including FDA reporting activities

+ Coordinate with IRBs, FDA, investigators, sponsors, and CROs

+ Oversee multi-site clinical trials, ensuring adherence to regulatory timelines and accuracy

+ Prepare and submit:

+ New study protocols, amendments, and continuing reviews

+ Informed consent forms and updates

+ Regulatory reports and essential documentation


+ Ensure compliance with ICH/GCP guidelines, FDA regulations, and AAHRPP sta...

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