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needed. Provide education and training to clinical staff on research protocols and procedures. Develop study-specific tools and manage biological specimen collection, processing, and shipping. Maintain
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. Ensure the consent process is performed in compliance with institutional, FDA, IRB, clinical trial sponsor and other applicable regulations.
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. Additional responsibilities might be to oversee an MSAT team. As a successful candidate you will: · Oversee day to day activities related to facility and support as needed to ensure smooth operation of
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recruitment and pre-screening. Develop strategies for identifying potentially eligible patients for each study. Present trial concepts to research subjects and participate in the informed consent process
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, including logs for facility and equipment maintenance, autoclaves, RO systems, and cage wash operations. Research Support Assist investigators with setting up animal housing and procedure rooms, fogging
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OnCore calendar builds to ensure timeliness and accuracy. The PM plays a significant role in supporting a timely study start process and is responsible for collecting and provide sponsors with regulatory
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efficiency, regulatory compliance, and study oversight. In this role, you will be responsible for attending clinics as needed, ensuring smooth data compilation, registration, and submission processes. You will
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for identifying potentially eligible patients for each study. The CRN presents trial concepts and details to the research subjects, participates in the informed consent process, enrolls, and coordinates care
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, regulatory compliance, and study oversight. In this role, you will be responsible for attending clinics as needed, ensuring smooth data compilation, registration, and submission processes. You will monitor
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deciphering their underlying molecular mechanisms in normal developmental processes and tumorigenesis. We cover research areas with relevance to RNA Biology, Cancer Biology, Chromatin Regulation, Cancer