We are seeking an Informed Consent/Protocol Editor for our growing Team! Responsible for editing and writing informed consent documents, protocols, and standard text for MSK's clinical research protocols in accordance with institutional policies, federal regulatory standards, and ease of understanding by research participants. Ensures that documents are written/edited to the expectations and standards set forth by the Protocol Activation Unit, IRB members, and research sponsors. Makes improvements to documents based on content, language, complexity, and reading level. You will: Edit informed consent documents, protocols, and other protocol materials for reading level. Fact-check and cross-check info
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