Oversee regulatory operations of clinical studies for one or more disease and modality teams This includes internal investigatorinitiated studies external eg NCI and industrial protocols pharmaceutical and biotechnology company studies Requirements Bachelors degree required Masters Degree preferred 1 year of related work experience Experience in working with FDA regulations and guidelines 21 CFR ICH guideline and initiatives governing regulatory operations and submissions Pharma Biotech Medical Devices Previous working or educational experience in the field regulatory reporting and compliance ...
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