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. Prepare, maintain, and submit regulatory documentation to institutional and study oversight committees, including IRB, DSMB, and PRMC/CPRMC. Compile, review, and submit study data using protocol-specific
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participants are appropriately registered and maintain documentation of participant registration. Compile and submit data on appropriate forms according to protocol requirements. Ensure protocol compliance
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and academic career development. For more information about Dr. You’s lab, please visit here. As a successful candidate, you will: Lead independent and collaborative projects investigating the molecular
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the pathogenesis and pharmacogenomics of pancreatic cancer in order to accelerate treatment. Using a combination of molecular and genomic data and human-in-mouse models, the lab has identified four core subtypes in
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highly motivated postdoctoral fellow. For more information about Dr. Yang lab, please visit here. As a successful candidate you will: Study transcriptional regulation and RNA metabolism in normal
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multiple clinical research protocols to ensure efficient study conduct, regulatory compliance, accurate documentation, and timely data collection. Your responsibilities will include participant prescreening
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process. We will not request sensitive personal or financial information prior to the acceptance of a formal offer. All communications will come from official @coh.org email addresses. Interviews
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that patients are appropriately scheduled and registered; maintain documentation of patient registration. Compile and submit data on appropriate forms according to protocol requirements. Help train and mentor new
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documentation of participant registration. · Compile and submit data on appropriate forms according to protocol requirements. · Perform protocol specific clinical duties as required per
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. The lab employs a combination of cellular and molecular techniques, mouse models and patient samples to assess these areas. For more information on Dr. Vasavada’s research please visit here .