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plans on individual projects as well as directing research programs. This position reports directly to the Director of the Institute for Advancing Medical Innovation (IAMI). This position will be located
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Science. Position collaborates with cross-functional teams and monitors the progress and performance of all aspects of the assigned projects, including regular interactions with NIH Program Office. The
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and includes health expense accounts with generous employer contributions if the employee participates in a qualifying health plan. Employer-paid life insurance, long-term disability insurance, and
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for quality improvement and opportunities. Attend, and if applicable, coordinate meetings to facilitate on-going program management and development. This job description is not designed to cover or contain a
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: The Regulatory Coordinator is responsible for performing study-specific regulatory and safety reporting across multiple studies. This will be accomplished by: assuring the research is compliant with applicable
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requirements of the study. Scheduling: Assist the study coordinator with scheduling study visits Communicate with all parties involved, including the participant and caregiver (when applicable) as
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an expansive clinical trials program, actively recruiting to investigator-initiated, NRG, and NCI-based clinical trials ranging from early to late phase, being one of a few institutions with gynecologic oncology
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or on behalf of other investigators and clinical trials, in accordance with all applicable standard operating procedures (SOPs). Perform specimen banking for long-term storage for the repository or other
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protocol criteria and reviewing study documentation to ensure compliance with GCP guidelines and FDA CFR. Work closely with the Research Institute and Human Research Protection Program and have a working
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Department: SOM KC Office of Medical Education (OME) ----- Phase I Position Title: Program Manager, Medical Education Job Family Group: Professional Staff Job Description Summary: The Program