What are the responsibilities and job description for the Clinical Research Coordinator Intermediate (Underfill to Clinical Research Coordinator Associate) position at University of Michigan?
Clinical Research Coordinator Intermediate (Underfill to Clinical Research Coordinator Associate)
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How to Apply
A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position.
Job Summary
Provide all aspects of clinical research coordination.
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
Manage all aspects of assigned clinical trials including but not limited to :
IRB submissions, enrolling, consenting research subjects. Completing all aspects of assigned trials CRF submission, query resolution, IRB reporting including AE and or ORIO. Develop processes and tools to capture data in accordance with ALCOA -C principles.
Study binder creating and maintenance.
Sponsor communications, sponsor related activities such as SIV scheduling, monitoring scheduling and set up.
Working with internal auditors such as MICHR, Office of Research Compliance and departmental audits.
Self-audit assigned trials and assist with auditing other radiology studies.
Cross coverage on additional trials.
Required Qualifications
Intermediate :
Bachelor's degree in Health Science or an equivalent combination of related education and experience.
ACRP or SOCRA certification for clinical coordinators. Minimum of 3 years direct experience in clinical research and clinical trials is necessary.
Proficient in research protocol submissions. Experience with Rad-Cap and excel databases.
Ability to communicate concise, accurate information both verbally and written.
Associate :
Bachelor's degree in Health Science or an equivalent combination of related education and experience.
ACRP or SOCRA certification for clinical coordinators. Minimum of 2 years direct experience in clinical research and clinical trials is necessary.
Proficient in research protocol submissions. Experience with Rad-Cap and excel databases.
Ability to communicate concise, accurate information both verbally and written.
Desired Qualifications
Excellent verbal and written communications. Proven excellent customer service. Ability to foresee needs of faculty and staff they support and respond accordingly. Critical thinking skills. Ability to quickly understand detailed protocols and develop CRFs, and databases accordingly.
Work Schedule
40 hours per week; 9 : 00-5 : 00
Work Locations
VV (Victor Vaughn Building)
Modes of Work
Positions that are eligible for hybrid or mobile / remote work mode are at the discretion of the hiring department. Work agreements are reviewed annually at a minimum and are subject to change at any time, and for any reason, throughout the course of employment. Learn more about thework modes (https : / / hr.umich.edu / working-u-m / my-employment / ways-we-work-resource-center / ways-we-work-implementation-group / modes-work) .
Underfill Statement
This position may be underfilled at a lower classification depending on the qualifications of the selected candidate.
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
258596
Working Title
Clinical Research Coordinator Intermediate (Underfill to Clinical Research Coordinator Associate)
Job Title
Clinical Research Coord Inter
Work Location
Ann Arbor Campus
Ann Arbor, MI
Modes of Work
Onsite
Full / Part Time
Full-Time
Regular / Temporary
Regular
FLSA Status
Exempt
Organizational Group
Medical School
Department
MM Department of Radiology
Posting Begin / End Date
2 / 11 / 2025 - 2 / 28 / 2025
Career Interest
Radiology
Research
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