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scientific research. Primary Responsibilities • Perform and develop routine and complex experimental designs for implementation in the lab. • Develop new methodologies for lab procedures. • Oversee
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and animal models. Develop and optimize siRNA formulations and encapsulation strategies in lipid- or nanoparticle-based delivery systems. Perform in vivo testing of siRNA-loaded nanoliposomes in disease
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support staff on pre-trial functions including budget development, contract negotiations and IRB applications. Advise department study investigators and support staff on administrative and regulatory
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functions including budget development, contract negotiations, IRB applications, FDA regulations, and grant development. Advise department study investigators and support staff on administrative and
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independence through the development of professional skills that enable the postdoc to actively pursue a career of his/her own choosing. Be supervised by at least one senior scholar who actively promotes
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to develop new ideas by analyzing complex, multi-faceted information. Ability to prioritize multiple assignments and deadlines. Technical knowledge of FERPA, F-1 visa regulations and J-1 program
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training, and meet regulatory requirements, including those of the privileging institution, CMS, and the Joint Commission Evaluate quality outcomes for patients through participation in the development
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Position Description: Summary Assist in the fabrication, construction, and testing of experimental systems in accordance with research protocols to develop new techniques. Assist with running
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investigators. Assure compliance with all relevant IRB and other regulatory agency requirements. Prepare IRB documents and reports. Assist in the evaluation and writing of research protocols. Collaborate
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leads the development, and support of Workday reporting and data analytics needs across all Workday modules. This role ensures that reporting and data needs align with institutional goals, performance