Job Information
University of Michigan Clinical Research Technician / Assistant (underfill) in Ann Arbor, Michigan
Clinical Research Technician / Assistant (underfill)
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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 Clinical Research Technician position is required.
The Research Study Coordinator will play a crucial role in supporting clinical studies by facilitating patient recruitment, enrollment, and retention. This role includes direct patient engagement, data management, and administrative responsibilities to ensure compliance with study protocols and institutional guidelines. This position requires full-time, in-person engagement and reports to three Principal Investigators (PIs) in a collaborative leadership structure.
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*
This role offers an excellent opportunity for growth within the clinical research field, providing hands-on experience with patient care, data management, and regulatory compliance in clinical research. The in-person requirement facilitates direct interaction with patients and research staff, essential for optimal study execution.
Experience as part of a team with 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
Essential Functions & Job Duties:
Patient Recruitment and Enrollment
Actively recruit potential participants for clinical studies through direct outreach, patient database searches, and by liaising with clinical teams.
Coordinate pre-screening, eligibility assessment, informed consent, and enrollment of study participants.
Provide participants with information regarding study protocols, ensuring that they fully understand the requirements, risks, and benefits of the study.
Longitudinal Patient Follow-up:
Maintain regular contact with study participants throughout the study to monitor adherence, schedule follow-up visits, and manage any concerns.
Conduct in-person or phone follow-up visits as specified in the study protocol, documenting any changes in participant health status, adverse events, or compliance issues.
Data Entry and Management:
Accurately enter patient data into REDCap or other study databases in real time, ensuring data integrity and completeness.
Conduct quality control checks and resolve any discrepancies in data entries.
Generate and submit data reports as required by study protocols and PI requests.
Regulatory and Compliance Management:
Prepare and submit initial IRB applications, renewals, amendments, and any protocol deviation reports in a timely manner.
Monitor regulatory timelines and ensure that all study documentation complies with institutional and federal regulations.
Coordinate with the IRB, data safety monitoring board, and other regulatory bodies as needed.
Administrative and Study Coordination Support:
Schedule and coordinate study-related meetings, including with the PI team, clinical staff, and other research personnel.
Assist with the development and implementation of study protocols, case report forms, and other research materials.
Support grant and study budget management activities as needed.
Supervision Received: This position reports directly to three Principal Investigators, Dr. Bishu, Dr. Singh, and Dr. Lee, who collectively oversee the research projects. The coordinator will receive specific project assignments and oversight from each PI depending on the study?s needs. The PIs will meet regularly with the coordinator to provide feedback, set objectives, and address any study or protocol issues.
Supervision Exercised: none
Required Qualifications*
Technician Level:
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.
Assistant Level:
- High school diploma or GED is necessary.
Desired Qualifications*
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.
Technician Level:
- Bachelor?s degree in Health Science or an equivalent combination of related education and experience is desirable.
Assistant Level:
- Associate Degree in Health Science or an equivalent combination of related education and experience is desirable.
Work Schedule
This is a full time in person position.
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 the CRC-Assistant title based on selected candidates’ qualifications.
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
257074
Working Title
Clinical Research Technician / Assistant (underfill)
Job Title
Clinical Research Technician
Work Location
Ann Arbor Campus
Ann Arbor, MI
Modes of Work
Onsite
Full/Part Time
Full-Time
Regular/Temporary
Regular
FLSA Status
Nonexempt
Organizational Group
Medical School
Department
MM Int Med-Gastroenterology
Posting Begin/End Date
11/19/2024 - 11/26/2024
Career Interest
Research
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