Summary

This position is in the Section of Plastic Surgery in the Michigan Center for Hand Outcomes and Innovative Research (MCHOIR). The team consists of nearly 30 members, including faculty, fellows, research staff, and students. MCHOIR staff perform a wide array of clinical and health services research. Primary methodologies include decision analyses, large database studies, and clinical trials.

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 Work at Michigan?

Being part of something greater, of serving a larger mission of discovery and care that's the heart of what drives people to work at Michigan. In some way, great or small, every person here helps to advance this world-class institution. It's adding a purpose to your profession. Work at Michigan and become a victor for the greater good.

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*

* Assist in writing clinical research grants and protocols

* Collecting and managing data for clinical research projects

* Familiarity with administrative data, statistical programming and analysis, SAS, Stata and R packages.

* Screens and has oversight for the recruitment of subjects, collects, processes and analyzes data, and manage full- and part-time research assistants.

* Assists in the reporting of results and writing manuscripts for publication.

Independent knowledge, skills, and abilities within 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

Supervision Received: This position reports directly to (a CRC-Lead, CRC-Project Manager, a unit Administrator, Director, or Faculty Principal Investigator)

Supervision Exercised: None

Required Qualifications*

* Bachelors degree in Health Science or an equivalent combination of related education and experience is necessary.

* Certification is required through Association of Clinical Research Professionals (ACRP) as a Certified Clinical Research Coordinator (CCRC) or Society of Clinical Research Association (SOCRA) as a Certified Clinical Research Professionals (CCRP) or equivalent. Candidates must be eligible to register or take the exam at date of hire and the certification must be completed or passed etc. within six months of date of hire. (Please review eligibility criteria from SoCRA