Clinical Research Coord Inter

　　Apply Now

　　Summary

　　This clinical research coordinator (CRC) position may provide study coordination for multiple clinical research studies of any complexity. Coordinator experience and mastery of all job duties from the CRC-Associate position on the Michigan Medicine CRC Career Ladder (https://research.medicine.umich.edu/our-units/clinical-trials-support-office/clinical-research-coordinator-career-ladder) is required. This position should begin to serve on various clinical research committees at the University level. This position demonstrates advanced skills and knowledge along with the ability to support, guide, train, and demonstrate the implementation of study related activities. This position applies critical thinking and creative problem-solving skills across a wide variety of clinical studies. This position contributes to the development of new processes, procedures, and tools to enhance clinical research activities across the competency domains and conducts quality assurance/quality control checks on their work. This level of CRC continues to build on their competency foundation by making greater investments in their ongoing continuing education and professional development. Key behavioral competency descriptors include: Design, demonstrate, develop, guide, and support.

　　We are excited to recruit a full-time Clinical Research Coordinator to join our team in the Division of Gastroenterology and Hepatology at the University of Michigan in Ann Arbor.

　　Our team focuses on studies to help people with liver disease. The specific focus for this position will be to help manage projects related to cirrhosis funded by the NIH. The projects include a randomized clinical trial of a statin medication that has the potential to change the lives of people living with cirrhosis; and an observational cohort study that will be the first big study to define how people with early cirrhosis do over time. This position involves joining a growing team of a PI hepatologists (liver specialists) and two additional coordinators and a project manager.

　　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*

　　Expert level 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

　　Work typically occurs during the business hours of the week however some flexibility is possible

　　Verifying patient eligibility for studies via medical chart reviews

　　Recruiting patients for study participation and obtaining informed consent

　　Coordinating study visits with patients and hepatology providers

　　Performing data collection (face-to-face surveys, chart reviews) and data quality assurance checks

　　Performing sample collection and initial processing

　　Monitoring study inventory and purchasing supplies

　　Maintaining study data using REDCap (Research Electronic Data Capture) or other programs.

　　Preparing study reports, annual reviews, and Institutional Review Board documentation

　　Monitoring subject safety and evaluating protocol compliance

　　Assisting with data analysis and preparation of manuscripts and conference presentations

　　Supervision Received: This position receives direct supervision and reports directly to a Clinical Research Manager and Faculty Principal Investigator.

　　Supervision Exercised: Could provide Functional supervision (likely in limited capacity such as training) of staff in titles within the CRC Career Ladder.

　　Required Qualifications*

　　Bachelor's 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 fromSoCRA (https://www.socra.org/certification/certification-program/program-overview/) orACRP (https://acrpnet.org/certification/crc-certification/) )

　　Minimum 3 years of directly related experience in clinical research and clinical trials is necessary. Please review SoCRA'sDefinition of a Clinical Research Professional (https://www.socra.org/certification/certification-program/definition-of-a-clinical-research-professional/for) qualifying experience prior to applying.

　　Desired Qualifications*

　　6+ years of direct related experienceAdditional Information

　　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.

　　Background Screening

　　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.

　　Application Deadline

　　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.

　　U-M EEO/AA Statement

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

　　Job Detail

　　Job Opening ID

　　243951

　　Working Title

　　Clinical Research Coord Inter

　　Job Title

　　Clinical Research Coord Inter

　　Work Location

　　Ann Arbor Campus

　　Ann Arbor, MI

　　Full/Part Time

　　Full-Time

　　Regular/Temporary

　　Regular

　　FLSA Status

　　Exempt

　　Organizational Group

　　Medical School

　　Department

　　MM Int Med-Gastroenterology

　　Posting Begin/End Date

　　1/30/2024 - 3/03/2024

　　Career Interest

　　Research

　　Apply Now