Job Information
University of Michigan Clinical Research Technician in Ann Arbor, Michigan
Clinical Research Technician
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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
This position may independently provide study coordination for simple and moderately complex clinical research studies. As a member of a coordination team, this position may help support a portfolio of projects with varying levels of complexity. Mastery of all job duties from the CRC-Assistant position on the Michigan Medicine CRC Career Ladder is required.
This position is currently aiming to engage the clinical research coordinator in clinical trials evaluating novel treatments for diabetes, and reducing complications from diabetes.
The focus of the research will be on the following clinical trials and research studies:
PRECIDENTD Prevention of Cardiovascular and Diabetic Kidney Disease in Type 2 Diabetes ? a PCORI funded, Phase IV, large scale Pragmatic Clinical Trial comparing the effect of GLP-1 RA (or dual GIP/GLP-1 RA) to SGLT-2i agents to prevent the risk of cardiovascular disease and diabetic kidney disease in patients with Type 2 Diabetes.
A Prospective, Randomized, Double-Blind, Sham-Controlled, Multicenter, Pivotal Study to Assess the Efficacy of Revita? Duodenal Mucosal Resurfacing (DMR) on Body Weight Maintenance in Participants with Obesity and Who Have Achieved at Least 15% Weight Loss on Tirzepatide Obesity Pharmacotherapy (REMAIN-1)
Type 1 Diabetes Exchange (T1DX-QI)
Additional future opportunities may be available in TrialNet, the Teplizumab Registry, and the Long-Term Study of MODY-Monogenic Diabetes (University of Michigan's MODY Registry) if these are of interest to the applicant.
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*
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
Duties and Responsibilities:
Clinical Coordinator Responsibilities:
Performs study procedures with accuracy
Demonstrates ability to triage complex study concerns appropriately
Schedules, prepares for, and attends study initiation meetings, monitor visits, and audits.
Demonstrates ability to manage increasing levels of protocol complexity and/or volume efficiently.
Data Coordinator Responsibilities:
Contributes to the development of processes and tools to capture data in accordance with ALCOA-C principles
Demonstrates the ability to create CRFs, study documents, and tools
Demonstrates ability to resolve complicated queries
Monitors site compliance with subject safety reporting, escalates issues, and contributes to the development of tools and processes to enhance subject safety during the conduct of a clinical study.
Regulatory Responsibilities:
Provides logistic and regulatory guidance on FDA-regulated, Investigator-initiated research, and sponsor-initiated research studies.
Provides other administrative support for study activity (including, but not limited to subject reimbursement & payments)
Administrative & Training:
- Participates in training specific specifically for maintaining certification as a Clinical Research Professional
Supervision Received: This position reports directly to Faculty Principal Investigator.
Supervision Exercised: Could provide Functional supervision of staff within the CRC Career Ladder, temps and possible students.
Required Qualifications*
Associate degree in Health Science or an equivalent combination of related education and experience is necessary.
Minimum 1 year of directly related experience in clinical research and clinical trials is necessary. (Please review SoCRAs Definition of a Clinical Research Professional for qualifying experience prior to applying.) or An advanced degree in a health-related areas such as: Health Sciences, Behavioral Sciences, Public Health, Health Care Administration, Clinical Research Administration, Social Work, Psychology, Epidemiology, Foreign MD. or Minimum 3 years of human subject experience (clinical, lab or health regulations) such as related patient care, related community health and wellness, related clinical information, and research.
Desired Qualifications*
Bachelors 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
This is a full-time position; remote work is an option.
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) .
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
257907
Working Title
Clinical Research Technician
Job Title
Clinical Research Technician
Work Location
Ann Arbor Campus
Ann Arbor, MI
Modes of Work
Hybrid
Full/Part Time
Full-Time
Regular/Temporary
Regular
FLSA Status
Nonexempt
Organizational Group
Medical School
Department
MM Metabolism, Endo & Diabetes
Posting Begin/End Date
12/13/2024 - 12/20/2024
Career Interest
Research
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