Hiring: PS Project Administrator Company: University of Utah Location: Salt Lake City, UT Job Posted Time: 2026-09-10 13:21:05 Employment Type: Full-time Target Skills & Keywords : Program Management About the job Required Skills: •Oversees all administrative, financial, personnel, and technical functions of a program in an assigned department. Organizes and assigns duties to employees and advises the departmental administrators of the program's activities. •Huntsman Cancer Institute is committed to cancer prevention, care, and survivorship for all communities within the area we serve – which includes Idaho, Montana, Nevada, Utah, and Wyoming – with impact worldwide. •Supports Principal Investigators (PI) and study management staff with patient screening/enrollment, eligibility review, data submission, and overall maintenance of new and ongoing clinical trials. •Ensures study management staff are providing quality source documents and data to sponsors, while ensuring protocol compliance is maintained within regulatory guidelines and standards. •Routinely monitor and ensure compliance with eligibility, protocol requirements, data submission completion while monitoring delinquency rates, outstanding query resolutions •Ensure monitoring/auditing reports and outstanding issues with staff are identified, addressed, and resolved in appropriate timeframe while providing direction and oversight. •Provides assistance with personnel management and supervision, while mentoring and training new or junior research staff and providing adequate team coverage plans. •Contribute to developing educational materials on coordination and data completion processes and requirements for the teams, as well as evaluation and education tools to assess staff competency. Qualifications: •Background knowledge of assigned department's area of specialization in order to analyze, plan, train and draw conclusions for recommendations to Clinical Trial Manager. Demonstrated leadership skills in planning and directing employees and processes in order to effectively monitor and develop team and to ensure the smooth operation of department. •Completion of provided supervisory/management training within one year of employment may be required. •Three years of Oncology Clinical Research Coordinator Experience •Advanced knowledge and understanding of regulatory guidelines related to human subject research protections in clinical trial investigations •Clinical Trial Management Software experience •Demonstrated capacity to assess functional processes, workflow and develop improvements for efficiency and quality output. •Advanced knowledge of industry standards related to clinical trial coordinator functions and study data management activities; (i.e., complex trial designs, data standards, data reviews, etc.). •Demonstrated ability to positively influence others in a team environment •Full Time or Part Time? Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!