We are seeking a Lead Informed Consent/Protocol Editor for our growing Clinical Research Team. You will: Be responsible for editing informed consent documents, protocols, and standard text to ensure compliance with MSK IRB requirements and with regulatory standards for MSK clinical research protocols. Ensure that the scientific language of the consent form is easily understood by research participants. Ensure that documents are written/edited in compliance with the standards established by the Protocol Activation Unit, the MSK IRB, and industry sponsors to reduce the need for modifications based on content, complexity, and reading level. Help develop standard text libraries for consent document
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