Research - Laboratory/Non-Laboratory, Staff/Administrative
Research Project Coordination (80%) • Assists with supporting a large and complex portfolio of research projects • Facilitate patient participation in clinical research, including: o Screening and recruiting patients and families o Ensuring study eligibility and enrollment o Scheduling and conducting research visits • Data management for multiple projects, including: o Data collection and entry into databases o Ensuring data quality o Supporting the PI and Developer in database development • Specimen management for multiple projects, including: o Facilitating the collection of research specimens during routine clinical procedures o Ensuring high quality processing of research specimens o Assist in coordinating timely and compliant shipment of research specimens to research laboratories • Provide information to University faculty and staff for protocol specific queries, including availability of trials, enrollment requirements, specimens needed, etc. • Engage with the research team in verifying subject eligibility, facilitating subject enrollments, and ensuring compliant completion of research activities • Support timely and accurate data submission; engage with providers and investigators to ensure adequate source documentation is available; accurate interpretation and recording of data; maintenance of subject research charts • Facilitate the timely review and reporting of adverse reactions and serious adverse events
Research Regulatory Management (10%) • Support the team with regulatory tasks as assigned • Support the completion of required regulatory documentation • In collaboration with the research team, interpret study protocols and inform the development of consent forms and other participant materials needed for each clinical research study • Support the team in maintaining regulatory binders and required documentation for each clinical research study to ensure compliance and to be audit-ready at any given time • Prepare for and participate in site initiation visits, monitoring visits, program audits, etc. • Report Unanticipated Problems according to University policy
Administration (5%) • Facilitate new project development and start-up activities • Support quality improvement initiatives • Attend national and study meetings as appropriate
Education (5%) • Educate University faculty and staff of our regulatory and research obligations in relation to our clinical research activities • Communicate with clinical teams to foster an environment of quality research participation within the context of exceptional clinical care
All required qualifications must be documented on application materials
Required Qualifications: • BA/BS in a scientific or health related field, OR a combination of education and experience to equal 4 years • Experience with computerized data management, preferably in a health-related setting, including electronic medical records • Demonstrated data management skills, such as data collection, data entry and quality control • Computer proficiency and ability to navigate multiple software applications • Detail-oriented with exceptional organizational, planning and problem-solving skills • Ability to work independently, as well as part of a team • Ability to adapt to changing priorities based on most critical need • Demonstrated ability to maintain deadlines and prioritize assignments • Excellent written, verbal and interpersonal skills • Ability to work flexible work hours, including occasional evening and weekends • During a typical 8 hour shift, a person in this position may be required to stand up to 2.5 hours, walk up to 2.5 hours (including stairs), reach above shoulders, lift up to 10 pounds above the shoulder, and carry packages across campus at waist level.
Preferred Qualifications: • Experience working with patients and families, preferably within a hospital setting and/or pediatric populations • Knowledge of federal regulations related to research with human subjects and protected health information • Certified Medical Assistant or similar experience • Clinical research experience • Specimen management experience including processing human samples and shipping per regulations
Internal Number: 340877
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.