Research Professional 3: General Internal Medicine
University of Minnesota, Twin Cities
Location: Minneapolis, Minnesota
Salary: 46696.00 - 79393.60
Internal Number: 342880
This position will be the primary manager of day to day operations for remotely delivered clinical trials, including the ACTIV 6 study. This study is funded by NIH and it is critical that study activities have an experienced study manager to support the scientific efforts of Dr. Bramante as study PI.
Description Primary Responsibilities:
-Assist PIs with research, coordination, administration, planning and implementation of study; - Lead and monitor data collection activities; - Anticipate and resolve problems; - Applicant will participate in all phases and aspects of research; - "Dotted Line" Supervise and participate in a team of ~3 or more others working on the study; - Prepare REDCAP electronic data forms; - Prepare reports regarding study progress for the study team; - Organize investigator team meetings; - Coordinate UMN and other site study activities; - Manage IRB communications (or interface with the CTSI, who is handling most of the IRB work); -Interface with the CTSI team who is helping with ct.gov account; - Assist with preparation of progress reports for funders; - Assist with administration of informed consent as schedule demands; - Assist with data entry and distributing study supplies as schedule demands; - Assist with presenting research findings; - Support PIs' interactions with the departmental accountant to ensure fiscal reporting and budgetary management of the project, including purchases for the study; - Promptly contact the PIs for potentially serious adverse events; - Ensure compliance with human subjects, HIPAA, participant consent, and study personnel training requirements, and other regulations.
Be available during weekends and evenings approximately once every 8 weeks, with advanced notice.
All required qualifications must be documented on application materials
Required Qualifications: 1) Bachelor's degree plus at least four years of related experience or a similar combination of education and experience to total eight years. 2) Proficiency with Microsoft Word, Excel, Powerpoint, Google Drive, and experience with REDCap. 3) Prior quantitative research experience including clinical trials research involving direct patient contact, data collection, and interfacing with team members. 4) Experience following IRB/HIPAA guidelines. 5) Ability to read and communicate in English. 6) Excellent organization skills with attention to detail. 7) Demonstrated interpersonal and communication skills. 8) Able to work independently. 9) Proven track record of reliability.
Preferred Qualifications: 1) BS/BA in a health-related field. 2) Additional professional experience on a clinical research project team or similar environment. 3) Experience in an academic medicine setting.
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.