A cover letter is required for consideration for this position and should be attached as the first page of the resume. The cover letter should address the specific interest in the position and outline skills and experience that directly relate to this position. To be considered for this position, the applicant must have met all the required qualifications before the employment start date.

The Michigan Alzheimer's Disease Center (MADC) is an NIH-funded research center focused on conducting and supporting Alzheimer's disease and related dementia research. A key aim of the center's research is to work with underrepresented communities to address racial and ethnic disparities in Alzheimer's disease and related dementias. The center also spans beyond research by promoting state-of-the-art care and wellness for individuals and families affected by dementia and increasing dementia awareness through education and outreach across the state.

The Michigan Alzheimer's Disease Center is seeking a full-time Imaging Research Assistant to join the research team within the Neuroimaging Core. The position is in Ann Arbor with free staff parking. 

Reporting to the MADC Neuroimaging Manager, the successful candidate will be able to operate in a semi-independent manner and collaborate with research administrative staff, the Neuroimaging Core Manager, and the Imaging Research Coordinator. The role involves assisting in the logistics and technical aspects of imaging studies involving research study participants and the candidate in this role will be able to carry out a range of tasks associated with a variety of research studies. The characteristic duties and responsibilities of this position may evolve over time to match changing needs and priorities.

This position may independently provide study coordination for simple and moderately complex clinical research studies.  As a member of a coordination team, this position may help support a portfolio of projects with varying levels of complexity. Mastery of all job duties from the CRC-Assistant position on the Michigan Medicine CRC Career Ladder is required.

• Experience as part of a team with all 8 competency domains is expected:
  • Scientific Concepts and Research Design
  • Ethical Participant Safety Considerations 
  • Investigational Products Development and Regulation
  • Clinical Study Operations (GCPs)
  • Study and Site Management
  • Data Management and Informatics
  • Leadership and Professionalism
  • Communication and Teamwork
• Coordinate research participant scheduling and communication, including calling, scheduling, and mailing appointment reminders.
• Conduct imaging safety screenings with participants and record pertinent information.
• Safely transport participants between U-M research sites using U-M leased vehicles, when required.
• Monitor and record key details of MRI/PET scans, including start/end times, duration, completion status, and any issues encountered.
• Administer computerized tests to participants for functional MRI data collection.
• Assist with MRI/PET slot scheduling with imaging technologists monthly.
• Maintain and organize study data forms, ensuring high standards of data quality and control.
• Enter data into relevant databases and assist with data management.
• Collaborate effectively with various teams within MADC, Neurology, and Neuropsychology clinical trials.

Supervision Received: 

This position receives direct supervision and reports directly to the Neuroimaging Core Manager. 

Supervision Exercised: 

None.

• High school diploma or equivalent.
• Proficiency with standard computer programs, (i.e., Microsoft Office Suite, Outlook, Google Suite).
• Excellent multitasking ability and strong record-keeping skills.
• Highly motivated and capable of working independently with minimal supervision.
• Ability to work with diverse teams of people in a collaborative and effective manner. 
• Ability to problem-solve and establish timelines and priorities independently.

• Associate's degree or equivalent combination of education and experience.
• 1 year of clinical research experience or relevant experience.
• Experience in working with research participants, particularly older adults with or without memory loss.
• Familiarity with investigator-initiated and federal sponsored trials.
• Proficiency in Electronic Data Entry, preferably in REDCap or a similar platform.
• Understanding of Good Clinical Practice and HIPAA regulations.
• Knowledge of medical terminology and laboratory value assessment.
• PEERRS or CITI Program certification.

Positions that are eligible for hybrid or mobile/remote work mode are at the discretion of the hiring department. Work agreements are reviewed annually at a minimum and are subject to change at any time, and for any reason, throughout the course of employment. Learn more about the work modes.

Michigan Medicine is firmly committed to advancing inclusion, diversity, equity, accessibility, and belonging, which are core to the culture and values of the Medical School Office of Research. Our community supports recruiting and cultivating a diverse workforce as a reflection of our commitment to serve the diverse people of Michigan and the world. We strive to create a work culture where each team member feels respected, valued, and safe.

Michigan Medicine conducts background screening and pre-employment drug testing on job candidates upon acceptance of a contingent job offer and may use a third party administrator to conduct background screenings.  Background screenings are performed in compliance with the Fair Credit Report Act. Pre-employment drug testing applies to all selected candidates, including new or additional faculty and staff appointments, as well as transfers from other U-M campuses.

Job openings are posted for a minimum of seven calendar days.  The review and selection process may begin as early as the eighth day after posting. This opening may be removed from posting boards and filled anytime after the minimum posting period has ended.

The University of Michigan is an equal opportunity/affirmative action employer.