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as required and ensures protocol is followed. May prepare IRB submissions. May process, ship, track or otherwise handle research specimens. QualificationsEmpty heading Required: Associate. Degree
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) and local Institutional Review Board (IRB). Primary Duties and Responsibilities Provides research writing activities such as developing scientific documents for abstracts, publications, presentations
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accurate; assist with query resolution in a timely manner. Document and report serious adverse events per protocol and institutional policy. Act as a liaison with hospital staff, physicians, IRB, review
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subcontractors; conducts literature searches and literature reviews; assists with institutional review board (IRB) applications and other data governance requests; designs and executes linkage strategies
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research coordinators and involves direct interactions with the UChicago Office of Clinical Research (OCR), the Clinical Trials office, and the Institutional Review Board (IRB). The clinical research studies
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Benefits TTI employees can choose from several health coverage options offered by The Texas A&M University System for themselves and their families, as well as numerous other benefit programs. https
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research safety standards. Data and Regulatory Compliance Maintains study documentation and research records in accordance with institutional policy, sponsor requirements, and federal regulations (IRB, FDA
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a resource to other Cancer Institute faculty and staff on available protocols, and general research topics such as FDA, IRB and GCP regulations. Essential Duties and Responsibilities include
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resource to other Cancer Institute faculty and staff on available protocols, and general research topics such as FDA, IRB and GCP regulations. Essential Duties and Responsibilities include the following
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(IRB) protocols for research including clinical trials and retrospective studies Coordinate staff in ensuring all regulatory requirements are met and documented for clinical trials, including but not