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Clinical Research Coord Inter/Assoc/Technician
Clinical Research Coord Inter/Assoc/Technician-March 2024
Ann Arbor
Mar 29, 2026
About Clinical Research Coord Inter/Assoc/Technician

  Clinical Research Coord Inter/Assoc/Technician

  Extended Site Maintenance

  We are performing updates and maintenance to our applicant experience. As a result, the site will be unavailable Saturday, January 27th at 9pm EST through Sunday, January 28th at 7:30am EST. During this outage period, applications for job postings can not be submitted.

  Apply Now

  Summary

  The University of Michigan MATRIx team provides transcatheter (catheter-based) therapies for Mitral and Tricuspid valve disease. The MATRIx multidisciplinary team includes interventional cardiologist, cardiac surgeons, nurse practitioners, registered nurses, and clinical research coordinators.

  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 one of the levels below (Intermediate, Associate, Technician) on the Michigan Medicine CRC 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.

  Responsibilities*

  Characteristic Duties and 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

  Responsibilities will include, but are not limited to:

  Assists in quality control efforts to ensure work integrity.

  Assists with startup activities; contributing to the development of tools and processes to enhance the administration and execution of clinical studies.

  Assesses protocols and troubleshoots for potential implementation issues.

  Executes routine study management activities.

  Performs study procedures with accuracy.

  Triages complex study concerns appropriately.

  Schedules, assists with preparation, and attends study-related meetings.

  Manages increasing levels of protocol or study complexity and/or volume efficiently.

  Works with the research administration in the department and/or CTSU to appropriately manage subject visits and reconcile financial activity of study participants.

  Resolves complicated queries.

  Takes an active role in ensuring data quality.

  Understands Investigational product development processes and applies key regulatory requirements to control these processes.

  Accurately identifies and reports AEs, SAEs, and ORIOs

  Fulfills regulatory requirements related to use of devices used in studies and procures devices for inventory.

  Supervision Received:

  This position reports directly to the Clinical Research Manager for the Department of Cardiac Surgery. This position will have functional supervision by the Structural Heart Research Manager.

  Supervision Exercised:

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

  Required Qualifications*

  Intermediate Level

  Bachelor's degree in health science or an equivalent combination of related education and experience is necessary.

  Certification is required through the Association of Clinical Research Professionals (ACRP) as a Certified Clinical Research Coordinator (CCRC) or the 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 or ACRP prior to applying.)

  Minimum of 3 years of directly related experience in clinical research and clinical trials is necessary at Intermediate level. (Please reviewSoCRA's Definition of a Clinical Research Professional for qualifying experience prior to applying.)

  Associate Level

  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 from SoCRA or ACRP prior to applying.)

  Minimum 2 years of directly related experience in clinical research and clinical trials is necessary. (Please reviewSoCRA's Definition of a Clinical Research Professional for qualifying experience prior to applying.)

  Technician Level

  Associate degree in health science or an equivalent combination of related education and experience is necessary.

  ONE of the following:

  ?

  Desired Qualifications*

  Intermediate Level

  6+ years of directly-related experience

  Experience working in a medical device or regulated industry

  Experience with electronic data capture

  Knowledge of cardiovascular physiology and structural heart anatomy

  Associate Level

  4+ years of direct related experienceTechnician Level

  Bachelor's degree in Health Science or an equivalent combination of related education and experience is desirable. An understanding of medical terminology, experience in a large complex health care setting, ability to effectively communicate with staff and faculty of all levels, and knowledge of university policies and procedures is desirable.Work Schedule

  Hours/Week: 40 hours

  Shift/Hours/Days: Days, occasional evening, potential weekends

  Underfill Statement

  This position may be underfilled at a lower classification depending on the qualifications of the selected candidate.

  Additional 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

  243525

  Working Title

  Clinical Research Coord Inter/Assoc/Technician

  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 Cardiac Surgery

  Posting Begin/End Date

  1/24/2024 - 2/14/2024

  Career Interest

  Research

  Apply Now

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