University of Utah · 1 day ago
Associate Director, Clinical Research Quality Assurance Management
University of Utah is seeking an Associate Director of Clinical Research Quality Assurance who will be responsible for the preparation, implementation, and coordination of research projects. The role involves ensuring compliance with protocols and managing quality assurance operations within clinical studies.
Higher Education
Responsibilities
Quality assurance and quality control of reading center operations. Ensure compliance with protocols, regulatory regulations, and overall objectives. Ensure that all targets, timelines, budgets, and requirements are met.Management of internal Quality Management System, revise and expand internal SOPs (Standard Operational Procedures)
Overview and perform study startup, budgeting and invoicing
Interact with the sponsors regarding organization of reading center services
Build, review, and maintain clinical databases, data collection tools, and applications, particularly based on Redcap databases
Serve as liaison with study sponsor and CRO as directed
Create, review, and maintain study documentation, such as Case Report Forms(CRFs) and Data Transfer Agreements (DTAs)
Compile, analyze, clean, and validate clinical trial data. Overview data transfers to the study sponsor
Identify and resolve discrepancies and issues with clinical data
Develop data management reports and monitor study status to ensure timelines are met
Conduct highly complex work, unsupervised and with extensive latitude for independent judgment
Assist UREAD staff members as necessary to meet the needs of the various studies
Qualification
Required
Requires a bachelor's (or equivalency) + 10 years or a master's (or equivalency) + 8 years of directly related work experience in clinical research and quality assurance
1 year of higher education can be substituted for 1 year of directly related work experience
Quality assurance and quality control of reading center operations
Ensure compliance with protocols, regulatory regulations, and overall objectives
Ensure that all targets, timelines, budgets, and requirements are met
Management of internal Quality Management System, revise and expand internal SOPs (Standard Operational Procedures)
Overview and perform study startup, budgeting and invoicing
Interact with the sponsors regarding organization of reading center services
Build, review, and maintain clinical databases, data collection tools, and applications, particularly based on Redcap databases
Serve as liaison with study sponsor and CRO as directed
Create, review, and maintain study documentation, such as Case Report Forms (CRFs) and Data Transfer Agreements (DTAs)
Compile, analyze, clean, and validate clinical trial data
Overview data transfers to the study sponsor
Identify and resolve discrepancies and issues with clinical data
Develop data management reports and monitor study status to ensure timelines are met
Conduct highly complex work, unsupervised and with extensive latitude for independent judgment
Assist UREAD staff members as necessary to meet the needs of the various studies
Preferred
Background in quality management and clinical research
Company
University of Utah
The University of Utah, located in Salt Lake City in the foothills of the Wasatch Mountains, is the flagship institution of higher learning in Utah.
H1B Sponsorship
University of Utah has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (216)
2024 (189)
2023 (201)
2022 (175)
2021 (156)
2020 (174)
Funding
Current Stage
Late StageLeadership Team
Recent News
National Institutes of Health (NIH)
2023-06-27
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