Meredith Cooper Email & Phone Number

Kansas City, Mo, Us

Kansas City, Mo, Us

Kansas City, Ks, Us

Kansas City, Ks, Us

Kansas City, Ks, Us

- Manages oncology accreditations and works with physicians and administrative leaders to ensure quality standards are met in accordance with standard requirements. - Develops relationships and provides guidance of quality and accreditation projects with both internal and external system partners.- Conducts in- depth assessment of qualitative and quantitative data. Collates information to support administrative and clinical decision making.- Assists in the development, analysis and maintenance of oncology quality dashboards, CGCAHPS and performance metrics. Supports and/or leads efforts to improve quality and performance metrics. - Manages projects within oncology department and various project teams. Ensures development of proper project plan within project management software is in place prior to project initiation and maintained throughout entirety of project.

Kansas City, Ks, Us

• Assure compliance with all relevant IRB and other regulatory agency requirements• Perform all functions necessary for initiation and/or completion of assigned research protocols• Assist in the administration of clinical research studies including documentation, collection and compilation of clinical research data• Serve as a liaison between Radiology Department and external department principal investigators and study staff• Review of all research protocols initiated through the KUMC Research Institute to determine role of Radiology in study activities

Durham, North Carolina, Us

• Provide comprehensive data management expertise to data management team for efficient, quality data to meet customer needs.• Assist in developing data test plans and specifying edits for datasets.• Ensure accuracy and timeliness of all data feeds received from participating laboratory vendors.• Train incoming Clinical Data Coordinators on roles and responsibilities during onboarding process

Durham, North Carolina, Us

• Managed day-to-day operations of study recruitment, adherence to standard operating procedures, screening medical records and consulting oncologists for study eligibility and executing study protocol to enroll and consent Stage IV cancer participants.• Developed source documents for IRB submissions, study compliance documentation, adverse event reporting, and updates for annual NIH report.• Assisted in the development and enhancement of study protocols and procedures as well as study intervention development.