University of Michigan · 9 hours ago
Clinical Research Technician
Ann Arbor, MI
Full-time
Onsite
Entry, Mid Level
1+ years expThe University of Michigan is one of the largest health care complexes in the world, and they are seeking a Clinical Research Technician to support the coordination of clinical trials at FNICOMO lab. The role involves coordinating studies, managing data, ensuring regulatory compliance, and performing administrative tasks related to clinical research.
E-LearningEducationHigher EducationUniversities
Responsibilities
Coordinates multiple studies both independently and as a member of a team
Screens and recruits subjects for several studies
Administers and scores neuropsychological test batteries to assess cognition, memory, and executive function
Evaluates participant motor and sensory functioning pre- and post-study drug intervention
Uses DEXA scanner to obtain bone density images
Trains subjects in the use of study devices. Triages any subject concerns
Monitors that study procedures and CRFs are completed accurately
Coordinates research procedures for complex clinical trials involving multiple MRI, PET, and lab appointments for each subject per study protocol
Utilizes MiChart to order participant imaging and research sample requests. Links orders to research to avoid billing errors
Performs wet lab procedures, such as centrifuging and aliquoting, to process biological specimens for internal and external use
Calculates and submits compensation to HSIP for subjects upon study completion
Creates and manages recruitment and enrollment tracking logs for multiple studies
Completes complex CRFs in accordance with ALCOA-C principles during study visits
Resolves data queries in CRFs for multiple studies
Develops and edits CRFs for Investigator Initiated trials
Manages the restructuring and maintenance of critical databases to streamline data entry and ensure that enrollment information is accurately stored
Transfers data from CRFs to databases
Prepares IRB applications, amendments, and continuing reviews
Collaborates with MICHR for INDs in clinical drug trials
Upholds the principles of Good Clinical Practice
Obtains informed consent both virtually using SignNow and in-person
Prepares materials for and participates in study initiation meetings, monitoring visits, and audits
Contributes to regulatory binder maintenance and data safety monitoring including AE and ORIO reporting
Revises and edits protocols and consent forms of varying complexity
Identifies potential research subjects using Data Direct, UM Health Research, and through community outreach
Communicates with subjects via phone, mail, and email
Schedules subject research visits and follow-up appointments
Adds appointments to the lab calendar
Orders prescription study drugs and maintains inventory logs
Coordinates the shipment of specimens to external sites
Keeps records of investigational drug inventories during clinical trials to maintain accountability and compliance with IRB requirements
Creates recruitment logs to track recruitment and retention
Creates advertisement flyers and study summary sheets for recruitment
Trains new research staff and student workers on test administration, data management and the use of lab equipment
Qualification
Required
Experience working with patients with neurodegenerative disorders, preferably Parkinson's disease
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 SoCRA's Definition of a Clinical Research Professional for 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
Preferred
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
Previous experience with clinical trial
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
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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
Recent News
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