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for its immune repertoire profiling program. The individual will be responsible for a) sample selection and study design, b) experimental protocols for data generation, and c) data analysis specifically
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Computational Sciences to lead a program in immune repertoire profiling, decoding, and analysis. The individual will manage multiple individuals at various ranks, providing support a) sample selection and study
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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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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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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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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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heavy use of multiple computer systems. The role provides continuity of care by ensuring a smooth transition between care settings and by developing a trusted relationship with patients to identify and
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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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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
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intercompany cost transfers (ICTs) Manage transfer price agreements (TPAs) for the research line of business Develop, implement, and maintain comprehensive procedure documents Facilities and Administrative (F&A