Hiring: PS Clinical Site Monitor Company: University of Utah Location: Salt Lake City, UT Job Posted Time: 2026-09-10 13:21:05 Employment Type: Full-time / Remote Target Skills & Keywords : Credentialing, GCP, Microsoft Excel, Microsoft Office, Microsoft PowerPoint, Project Management, Quality Assurance, Regulatory Compliance About the job Required Skills: •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. •Performs on-site and remote monitoring activities of clinical research studies. •Oversee, coordinate and conduct monitoring of clinical investigations to ensure compliance with University, Food and Drug Administration (FDA), Office of Human Research Protection (OHRP), Good Clinical Practice (GCP), state and federal guidelines. •Analyze and document monitoring processes for all activities in the conduct of the clinical investigation, and recommend improvements to operating policies and procedures for compliance review. Monitor and follow up on required documentation related to audit processes. •Develop and maintain site feasibility packets, multisite study procedural manuals, and other multisite process documents. •Prepare clinical sites for study start-up by conducting site initiation visits. •Analyze and evaluate data gathered during research. Identify data discrepancies and missing data in source records or CRF's. •Recognize protocol deviations and other study related issues and work to resolve and/or make appropriate recommendations for correction and full resolution. Qualifications: •Preferences include credentialing as a Certified Clinical Research Associate (CCRA), Certified Clinical Research Coordinator (CCRC), and/or Certified Clinical Research Professional (CCRP). Prior experience as an industry CRA or Monitor is also preferred. •Hiring department may require certification by an appropriate certifying body within two years of hire. •Applicants must demonstrate the potential ability to perform the essential functions of the job as outlined in the position description. •Oncology clinical trial experience highly preferred. •Solid functional working knowledge of Food and Drug Administration (FDA) requirements, Office of Human Research Protection (OHRP), International Conference of Humanization (ICH) Good Clinical Practice (GCP), as well as state and federal guidelines. •Knowledge of clinical development process sufficient to effectively direct and manage multiple projects and timelines. •Strong attention to detail, establishing priorities, and adhering to deadlines. •Able to show initiative and work independently, take initiative and complete tasks to meet deadlines. •Excellent interpersonal communication (including oral and written) and leadership skills also required. •Proficient in standard Microsoft office applications including Word, PowerPoint, Excel, Project, and other project management tools. Compensation: •Flexible work environment (work from home / hybrid options) 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!