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research. Knowledge of IRB and human research protection regulations required. Must have valid driver’s license and vehicle as occasional travel within NJ may be required. Preferred Qualifications Equipment
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-human, targeted therapy, immuno-oncology, and combination studies. Ensure protocol adherence and compliance with ICH-GCP, FDA regulations (21 CFR), IRB requirements, and institutional SOPs. Author and
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, IRB, and associated Modifications and Continuing Reviews. Monitor and track all study documentation to ensure timely execution and compliance and that information is correctly documented in
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