Michigan Medicine · 1 hour ago
Clinical Research Technician
Ann Arbor, MI
Full-time
Onsite
Entry, Mid Level
1+ years expMichigan Medicine is one of the largest health care complexes in the world, dedicated to improving the health of patients and communities through excellence in education, patient care, research, and technology development. The Clinical Research Technician will support the coordination of clinical trials at the FNICOMO lab, handling responsibilities that include coordinating studies, managing data, and ensuring compliance with regulatory standards.
EducationHealth CareMedical
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
Michigan Medicine
Michigan Medicine is a health care system and academic medical center that provides medical education and more. It is a sub-organization of University of Maichigan.
10001+ employees
Funding
Current Stage
Late StageLeadership Team
Heather Ascani
Director, Business Operations - Applied Systems Biology Core
Jack Kufahl
Chief Information Security Officer
Recent News
2025-12-11
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