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informed consent process or ensures that the informed consent process has occurred, is properly documented, and that informed consent form documents are filed as required. Interview prospective subjects
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account balances on a regular basis. Assists in completion of Internal Protocol Amendment Review forms. Helps with amendment treatment plans through the UCHealth Beacon process and works with assigned RN
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Manager, OCRST Program Coordinator Examples of Work Performed: IIT Program Oversight: 70% Oversee IIT protocol opening process across all pipeline studies, serve as a point of escalation, and intervene as
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systems to ensure appropriate activities have been logged; conduct ad hoc audits for compliance. Establish and define Process Improvement (PI) priorities as needed to ensure compliance and appropriate
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and research functions Utilize a variety of laboratory techniques required for research projects Perform experiments and tabulate and analyze research Support analytical testing process using standard
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current medication information, reviews research protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial Perform informed consent process or ensures
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current medication information, reviews research protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial Perform informed consent process or ensures
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medication information, reviews research protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial Perform informed consent process or ensures
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to applicants with disabilities throughout the employment application process. To request an accommodation pursuant to the Americans with Disabilities Act, please contact the Human Resources ADA Coordinator
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activities of the Office of DEIA - including but not limited to: Project timelines; Resources allocation/budgeting; Tracking of deliverables; and Process and activity/event evaluations. Work Location: Hybrid