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Clinical Research Coord Assoc/Tech/Asst

4 months ago

Ann Arbor, United States University Of Michigan Full time

Summary

The University of Michigans Division of Gastroenterology and Hepatology is seeking a motivated and organized Clinical Research Assistant to join our team. This position offers the opportunity to work under the guidance of Principal Investigators Dr. Shirley Cohen-Mekelburg and Dr. Jeffrey Berinstein, both of whom are early-career clinical researchers specializing in inflammatory bowel diseases. The successful candidate will play a crucial role in the management and operational success of both clinical trials and observational studies.

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*

Independent knowledge, skills, and abilities within 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

* Assist in the coordination and management of clinical research projects.
* Collect and manage patient and laboratory data.
* Develop and maintain research databases.
* Recruit and retain study subjects.
* Manage regulatory documentation and ensure compliance with all institutional and federal regulations related to clinical research.
* Support the Principal Investigators and research team in administrative tasks related to the research.

Supervision Received: This position reports directly to the Principal Investigators.

Supervision exercised: None

Required Qualifications*

Associate Level:

* 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