Job Abstract

Major responsibilities include 1) review language in research related agreements and 2) review and reconciliation of regulatory terms/issues in clinical trial agreements, IRB submissions, and informed consent forms. Reviews research related agreements (e.g. confidential disclosure agreements, clinical trial agreements, and subawards) provided by sponsors and negotiates the terms/language to comply with CUHC requirements. Reviews IRB submissions for funded studies and provides financial disclosur... more details

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