Job Description

Job Summary
This position provides administrative and coordination support for the conduct of clinical research projects. The candidate will provide support for the initiation and conduct of a new survey-based clinical study in critical illness survivors. This position is the entry level position on the Michigan Medicine CRC Career Ladder.

Mission Statement
Michigan Medicine improves the health of patients, populations and communities through excellence in education, patient care, community service, research and technology development, and through leadership activities in Michigan, nationally and internationally. Our mission is guided by our Strategic Principles and has three critical components; patient care, education and research that together enhance our contribution to society.

Why Join Michigan Medicine?
Michigan Medicine is one of the largest health care complexes in the world and has been the site of many groundbreaking medical and technological advancements since the opening of the U-M Medical School in 1850. Michigan Medicine is comprised of over 30,000 employees and our vision is to attract, inspire, and develop outstanding people in medicine, sciences, and healthcare to become one of the world’s most distinguished academic health systems. In some way, great or small, every person here helps to advance this world-class institution. Work at Michigan Medicine and become a victor for the greater good.

What Benefits can you Look Forward to?

Excellent medical, dental and vision coverage effective on your very first day
2:1 Match on retirement savings
Responsibilities*
Characteristic Duties and Responsibilities:
Knowledge of all 8 competency domains is expected:

1. Scientific Concepts and Research Design
2. Ethical Participant Safety Considerations
3. Investigational Products Development and Regulation
4. Clinical Study Operations (GCPs)
5. Study and Site Management
6. Data Management and Informatics
7. Leadership and Professionalism
8. Communication and Teamwork

Job Responsibilities:
Provide support for the initiation and conduct of human subjects research. This includes: liaison with other University collaborators, edit study-related documents, oversee regulation including IRB amendments and approvals and HIPAA compliance. Construct study survey and oversee the implementation of the survey including contacting eligible subjects, obtaining their consent, administering the survey, managing and analyzing the data, and assisting with preparing publications.

Supervision Received: This position receives direct supervision and reports directly to the Faculty Principal Investigator.

Supervision Exercised: None

Required Qualifications*
High school diploma or GED is necessary.
Desired Qualifications*
Undergraduate degree in a science or math field. Postgraduate degree (MS or PhD) in a biology, data science, or health sciences field is preferred. Experience with clinical care or clinical research is desirable.