<http://schema.org/description>
"...Protocol Development (and protocol related documents: inform consent form, amendments, study concept sheets, as appropriate). \u2022 Lead the clinical trial protocol development process in collaboration with CPO/Region representative (Medical Advisor, statistician, regulatory, etc.) or external expert recommended by customer. \u2022 Translating the approved trial concept sheets into executable clinical protocol (and Inform Consent Form) ready for customer \u201CProtocol Review Committee\u201D re-view/approval. \u2022..."^^<http://www.w3.org/2001/XMLSchema#string>
<https://tapwage.com/company/icahn-school-of-medicine-at-mount-sinai-department-of-oncological-sciences/science-writing/jobs>