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Clinical Research Coord Senior/ Intermediate
Michigan Medicine Ann Arbor, MI
$79k-108k (estimate)
Full Time 3 Weeks Ago
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Michigan Medicine is Hiring a Clinical Research Coord Senior/ Intermediate Near Ann Arbor, MI

SummaryEmergency Medicine is looking for an experienced Clinical Research Coordinator to lead a clinical research unit as part of the Weil Institute. The candidate will manage multiple study projects, in all aspects of clinical research including study planning, start up, IRB management, identifying study patients, consenting and enrolling participants, as well as data collection. The candidate will have oversight and mentorship over junior employees as well as oversight for clinical projects within the unit. The candidate will have the responsibility for ensuring that studies are completed within timelines. Primary activities and decision making will be performed independently affecting business operations to a substantial degree. Additionally, the candidate will be expected to meet with and work with study PIs. 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-Intermediate position on the Michigan Medicine CRC Career Ladder is required. This position gives back to the institution through mentoring others on study management and participating in training and development of junior clinical research professionals. This position demonstrates advanced skills and knowledge along with the ability to support, guide, train, and mentor study team members in the implementation of study related activities. This position applies critical thinking and creative problem-solving skills across a wide variety of clinical studies. This level of CRC develops new processes, procedures, tools, and training to enhance clinical research activities across the competency domains. This position 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, develop, evaluate, guide, mentor, and support.
Responsibilities*
Characteristic Duties And Responsibilities:Contribute to the development of process and tools in 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
  • Team lead for identifying, consenting, and enrolling subjects
  • Data management
  • Leading study meetings with faculty, staff, and clinical teams including start up meetings, study maintenance meetings, team meetings and study closeout.
  • Communicating with faculty, staff, and clinical teams
  • Mentoring junior staff
  • Other duties as assigned
Supervision Received: This position reports directly to a Senior Manager for Emergency Medicine.
Required Qualifications*
CRC Senior
  • CRC Governance Committee review and approval.
  • Bachelor's degree in Health Science or an equivalent combination of related education and experience.
  • 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)
  • Minimum 5 years of directly related experience in clinical research and clinical trials is necessary. Please review SoCRA's Definition of a Clinical Research Professional qualifying experience prior to applying.
CRC Intermediate:
  • Bachelor's degree in Health Science or an equivalent combination of related education and experience.
  • 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)
  • Minimum 3 years of directly related experience in clinical research and clinical trials. Please review SoCRA's Definition of a Clinical Research Professional qualifying experience prior to applying.
Desired Qualifications*
CRC Senior:
  • 9 years of direct related experience
CRC Intermediate:
  • 6 years of direct related experience
Work Schedule
Monday thru Friday 8am-5pm, hours may vary depending on the study with occasional weekends.
Underfill Statement
This position may be underfilled at the CRC-Intermediate title based on selected candidates qualifications and the review and approval of the Michigan Medicine CRC Governance Board.
Additional Information
The use of this title requires approval by the University of Michigan Clinical Research Coordinator Governance Board to ensure equity in title placement across Michigan Medicine.
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 Summary

JOB TYPE

Full Time

SALARY

$79k-108k (estimate)

POST DATE

06/03/2024

EXPIRATION DATE

07/25/2024

WEBSITE

uofmhealth.org

HEADQUARTERS

OAKLAND, CA

SIZE

15,000 - 50,000

FOUNDED

1869

TYPE

Private

REVENUE

$200M - $500M

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About Michigan Medicine

University of Michigan Health System owns and operates a network of hospitals and health centers that offers urology, cardiac and cancer care services.

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