University of Michigan · 15 hours ago
Clinical Research Technician
Ann Arbor, MI
Full-time
Onsite
Entry Level
1+ years expThe University of Michigan Kellogg Clinical Research Center is seeking a motivated Clinical Research Technician for a study on inherited retinal diseases. The role involves supporting research operations, including subject recruitment, data management, and regulatory compliance, while working closely with a team of specialists.
EducationE-LearningHigher EducationUniversities
Responsibilities
Help ensure that this study and others supported by the KCRC are initiated and executed in the highest quality and compliant manner
Play a pivotal role in maintaining day to day operations of this trial, including tasks related to subject recruitment, the administration of patient-reported outcome measures/instruments (PROs), and record keeping
Facilitate communications between team members, investigators, regulatory personnel, and other key contributors both in written and spoken form, using various software to document decision-making as needed
Relay study details to potential and enrolled participants, create written materials (e.g. letters, flyers, and consent documents), and assist with submissions and reports as required by the IRB, NIH, and other stakeholders
Communicate with sponsors, the University of Michigan Clinical Trials Support Unit (CTSU), and contract research organizations as applicable
Involved in data entry and organization, tracking screening, recruitment, randomization, and completion of participant activities, inputting data into REDCap, Excel, and case report forms (CRFs), maintaining studies in the OnCore clinical trial management system, and resolving queries
Follow all local, state, and federal regulations regarding clinical research in addition to Good Clinical Practice and protocol specific guidelines
Actively support an environment of strict regulatory compliance
Work within UM's eResearch regulatory system to create and revise IRB submissions, track any protocol deviations or adverse events and assure they are reported in a timely manner, and organize and store regulatory documents required by the NIH, UM, the Food and Drug Administration (FDA) and other regulatory authorities as required
Recruit and guide participants through study activities, including scheduling appointments with low vision and psychotherapy providers on the study team, conducting surveys, assessing suicidality, and assisting participants with accessing online materials and questionnaires
Possess a willingness to learn protocol specific requirements
Delegate tasks to full-time research interns, part-time temps, and undergraduate volunteers
Incorporate changes into the workflow as they occur
Qualification
Required
Associate degree in Health Science or an equivalent combination of related education and experience
ONE of the following: Minimum 1 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
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
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
Knowledge of general clinical research operations and regulations or a capacity to learn quickly
Ability to work both independently and as part of a team
Committed to prioritizing the welfare of the research volunteer
Exceptional organizational skills
Uncompromising integrity
Capacity to learn new skills as the positional needs change
Willingness to achieve professional certification such as SOCRA or equivalent
Experience with computers and applicable software (e.g. MS Word, Excel, Power Point, Outlook or equivalent)
Preferred
Bachelor's degree in Health Science or an equivalent combination of related education and experience
Experience working with patients in a healthcare setting and/or an understanding of medical terminology
Familiarity with terms related to psychology and/or an interest in research that involves psychological interventions
Ability to effectively communicate with staff and faculty of all levels
At least one year of directly related experience in clinical research and clinical trials
Knowledge of university policies and procedures
Experience with the MiChart (Epic) electronic health record (EHR) system
Experience with REDCap databases
Experience with the OnCore clinical trial management system (CTMS)
Ophthalmic technician skills (e.g. visual acuity, refraction, intraocular pressure, etc.) and phlebotomy skills or a willingness to learn as they may be needed in future studies
Willingness to accommodate occasional patient needs for contact outside of typical working hours
Benefits
Excellent medical, dental and vision coverage effective on your very first day
2:1 Match on retirement savings
Company
University of Michigan
The mission of the University of Michigan is to serve the people of Michigan and the world through preeminence in creating, communicating, preserving, and applying knowledge, art, and academic values, and in developing leaders and citizens who will challenge the present and enrich the future.
10001+ employees
H1B Sponsorship
University of Michigan has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (662)
2024 (594)
2023 (787)
2022 (473)
2021 (411)
2020 (324)
Funding
Current Stage
Late StageTotal Funding
$359.75MKey Investors
Michigan Economic Development CorporationNational Institutes of HealthBreakthrough T1D
2025-07-17Grant· $1M
2025-06-07Grant· $1.17M
2025-04-23Grant
Leadership Team
Greg McGuire
Managing Director, Mcity
Robert Goodspeed
Chair, Urban and Regional Planning Program
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