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and receiving appropriate feedback Fiscal Responsibilities: Charges for supplies and equipment appropriately. Role Development: Takes initiative and responsibility for identifying and pursuing learning
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, processing, and presentation. Perform computational analyses MHC class I peptide recognition, processing, and presentation. Responsibilities Engage fully with the projects and lab staff. Develop the ability
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. Responsibilities Project manage all aspects of the study startup process for clinical trials to include industry-sponsored, investigator initiated and grant funded trials. Identify research costs and develop and
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billing compliance. Act as protocol liaison with clinical teams, patients, and providers on study related topics. Prepare and coordinate monitoring visits and respond to queries and other requests from
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physical, emotional, social, and spiritual needs and evaluates patients' adaptation to health changes. Develops a plan of care based on patients' disease, symptoms, and response to treatment. Educates
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accordance with regulatory, GCP guidelines and institutional policy. Assist the Principal Investigator (PI) with protocol development, revision, and study analysis. Protocol Implementation Develop and maintain
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Science and Therapeutics Division and is a member of the Immunotherapy Integrated Research Center (IIRC). Their primary focus is on developing unique and first-in-class therapeutic drugs for cancer
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work on research projects related to TCR specificity and the endogenous and induced immune response to cancer and infections. Work will include developing innovative methods for TCR repertoire
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stronger. We seek employees who bring different and innovative ways of seeing the world and solving problems. Reporting to the Stuart and Molly Sloan Precision Oncology Institute Scientific Program Manager
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in the development, implementation and management of clinical trials. Responsible for the collection, coordination, processing, and quality control of clinical trial data in accordance with protocols