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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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study protocols, regulatory and GCP guidelines, and institutional policy. Develop and maintain tools for study implementation, including data collection tools, reference materials and specific study
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compliance Create timelines, monitor progress, and take necessary follow-up actions Regulatory Support Prepare and submit non-scientific portions of regulatory documents (e.g., IRB, IACUC, MTAs) Maintain up
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evaluates patients' adaptation to health changes Develops a plan of care based on patients' disease, symptoms, and response to treatment Educates patients, families, and caregivers on disease processes
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stakeholders, end users and team members throughout system development phases of assessment, design build, testing, training and implementation. As the primary individual responsible for implementation, support
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, and contracted staff on best practice prevention strategies to protect patients, care team members and visitors from risks of contamination or infection. Develops and provides education regarding
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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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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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relationships. In collaboration with the Principal Investigator, the Program Manager also contributes to long-term strategic planning, helping to set priorities and develop sustainable models for program growth
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finance budget activities including developing, analyzing, and monitoring clinical trial budgets and related operations under CRS. Responsibilities Prepare and project manage operating budgets based