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be conducted in person, in a clinical setting, the subject's residence, or by telephone. Coordinates the data collection process. May abstract data from the participant's medical record. Schedules
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Quarterly Business Review working sessions with key suppliers and key stakeholders and completes the annual supplier evaluation process and executes formal supplier development plans based on supplier
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program contacts. Tracks program expenditures, and may participate in the budget preparation process. May draft, edit and process grant proposals. Prepares and distributes reports. Coordinates logistical
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values representation from teaching-track faculty in College and University governance and service. Application procedure: Applications are submitted via INTERFOLIO https://apply.interfolio.com/177820 and
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safety and security for staff. Plans, develops, and implements organization-wide solutions for improved business processes, including identifying organization-wide systems to support operations. Ensures
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sensitive equipment, repairing electronics, editing data processing code, ordering supplies, backing up data on servers. Processes data according to defined protocols using specialized engineering software
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the budget planning process and prepare financial reports. May assist in identifying funding resources and developing fund-raising strategies and initiatives. Prepares operational and statistical reports
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FDA Good Clinical Practice (GCP) standards. KEY RESPONSIBILITIES: Provides clinical trials monitoring and follows established monitoring processes to support compliance with applicable regulations
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audits operations including laboratory procedures to ensure compliance with applicable regulations; provides leadership in identifying and implementing corrective actions/processes. Monitors IRB
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Professor (open track). An MD degree is required as is ABPN board certification (or in process of obtaining within 2 years of hire) in general psychiatry. NOTE: Position tasks are required to be performed in