Research Support - Laboratory/Non-Laboratory, Staff/Administrative
Job Duties/Responsibilities: - Subject and Data Management (60%) • Serve as liaison with clinics and offices to facilitate recruitment • Organize and maintain subject identification, recruitment, enrollment, and retention, including follow-up calls • Obtain data and accurately transit to appropriate database • Maintain study source documents • Organize, prioritize, and accomplish daily tasks related to research protocols • Assist in analysis of results; assist with development and submission of abstracts and publications - Regulatory Management (30%) • Support all aspects of human subject protection regulations: complete required IRB regulatory documentation, manage all IRB submissions and correspondence in conjunction with PI • Track and maintain all binders and regulatory documents -Research Lab Administration (10%) • Maintain research study database; obtain and publish updates of study progress • Coordinate study audits • Order Research supplies for the lab • Other tasks as assigned by the lab PI
All required qualifications must be documented on application materials
Required Qualifications: - BA/BS in a science-related field or a combination of related education and work experience to equal four years. - Experience recruiting, consenting and interacting with human research subjects, proven ability to recruit/retain subjects. - Troubleshooting and working independently skills are essential in this role. - Applies knowledge and skill to a recurring task or activity with emphasis typically on precision and timeliness of execution. • Ability to organize and manage several protocols concurrently • Ability to work flexible hours as required to recruit and enroll research subjects - Excellent attention to detail and ability to prioritize tasks - Strong problem solving and analytical skills - Ability to follow strict research protocols with utmost ethical standards - Knowledge of informed consent process and enrolling subjects with regards to established protocol, Good Clinical Practice, and University policies. - Experience with Office Suite, Google Apps, and web-based systems for tracking activities, calendaring, and retrieving/updating information - Possess excellent communication skills; oral and written - Strong team player
- 1-3 years working with patients in healthcare setting and/or clinical research experience. - Experience in the preparation of IRB applications and study-related documents - Familiarity with clinical research at the University of Minnesota, University of Minnesota Medical Center Fairview hospitals and clinics, and Veterans Administration Health Care System - Electronic medical record (i.e., EPIC), REDCap, and/or OnCore familiarity - Medical terminology knowledge - Background in neurosciences - Experience with data extraction
Internal Number: 340290
About University of Minnesota, Twin Cities
The University of Minnesota, founded in the belief that all people are enriched by understanding, is dedicated to the advancement of learning and the search for truth; to the sharing of this knowledge through education for a diverse community; and to the application of this knowledge to benefit the people of the state, the nation, and the world.