The Michigan Alzheimer?s Disease Center (MADC) is seeking a Clinical Research Assistant to join its research team. Hours are 40 per week, Monday-Friday. Location is at the Michigan Alzheimers Disease Center, 2101 Commonwealth Blvd, Suite D, Ann Arbor, MI, where there is free staff parking on site. This position is term limited to two years, with potential to extend dependent on future project funding.
This position is term limited to 2 years.
We are seeking an experienced, positive, highly motivated, organized, autonomous person with excellent multi-tasking ability and record-keeping skills to work with principal investigators and other research team members to accurately and efficiently carry out a range of tasks associated with a variety of research studies. The candidate will be able to operate in a semi-independent manner to assist in clinical research and related projects.
Job duties include coordinating and facilitating the timing of biospecimen collection for research patients with multiple study teams and integrating the workflow of many studies running simultaneously. Assist study teams with research study coordination including interacting with older, adult research participants and performing phlebotomy at the MADC in Ann Arbor, at the University of Michigan Detroit Center in Detroit, and other Center affiliated sites. Other duties include entering and managing research patient laboratory data, placing routine clinical laboratory research orders in EPIC MiChart, and processing biospecimens. This includes labeling, storing, handling and shipping specimens to NIH repositories, University of Michigan Pathology and maintaining lab supplies. Assist with special projects, in-services, evaluating new equipment and techniques, and other additional assigned responsibilities.
Knowledge of all 8 competency domains is expected and experience within applicable domains specific to unit needs.
- 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