Michigan Medicine · 6 hours ago
Clinical Research Coord Assoc/Technician/Assistant
Ann Arbor, MI
Full-time
Onsite
Entry, Mid, Senior Level
1+ years expMichigan Medicine is a leading health care complex known for its groundbreaking advancements and commitment to research and patient care. The Clinical Research Coordinator Associate role involves providing administrative study coordination and data entry support within the Oncology Clinical Trial Support Unit, ensuring compliance with clinical research protocols and effective management of clinical trials.
EducationHealth CareMedical
Responsibilities
Demonstrates understanding of protocol elements/requirements and demonstrates the ability to execute study procedures
Demonstrates the ability to anticipate and mitigate the potential for protocol non-compliance
Describes protocol structure and explains how to interpret study requirements to ensure study compliance
Demonstrates accurate implementation of protocol procedures
Explains and performs non-GCP-related study management activities
Performs study procedures with minimal supervision
Triages simple subject issues appropriately
Ensures integrity of specimen management (collection, processing, packing/shipping, storing, labeling, tracking, etc.)
Comfortable with basic clinical lab equipment such as a centrifuge, various freezers, pipettes, and standard laboratory safety requirements and guidelines
Explains the role of the Clinical Trial Support Unit (CTSU) for initiating new studies, and for subject visit billing
Performs moderately complex study procedures with accuracy
Triages simple subject concerns appropriately
Assesses studies for execution and troubleshoots potential implementation issues
Completes simple to moderately complex data collection during study visits
May work with CTSUs to reconcile financial accounts for study participants
Assists with local quality control efforts
Demonstrates the ability to screen participants for study eligibility
Performs simple study procedures with accuracy
Understands protocol structure and how to interpret study requirements to ensure study compliance
Understands proper documentation techniques, as outlined in the ICH-GCP guidelines
May complete simple study reimbursement with partners such as the Human Subjects Incentive Program (HSIP) and the CTSU finance team
Demonstrates the ability to find and utilize information from EMR and databases/CTMS/EDC
May mark visits as planned/occurred in OnCore
May provide lab results, not interpretation, to participants
May assist research coordinator in conduct of SIV; attends SIV
May assist in and attend monitor visits and/or audits
Qualification
Required
Bachelor's Degree in Health Science or equivalent in combined education and clinical research experience
Certification is required through Association of Clinical Research Professionals (ACRP) as a Certified Clinical Research Coordinator (CCRC) or Society of Clinical Research Association (SOCRA) as a Certified Clinical Research Professionals (CCRP) or equivalent. Candidates must be eligible to register or take the exam at date of hire and the certification must be completed or passed etc. within six months of date of hire. (Please review eligibility criteria from SoCRA or ACRP)
Minimum 2 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
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
High School Diploma or GED
Preferred
4+ years of direct related experience
Bachelor's Degree; Health Science field preferred or related certification
Understanding of medical terminology
Experience in a large, complex, healthcare setting
Ability to effectively communicate with staff and faculty of all levels
Knowledge of University policies and procedures
Bachelor's Degree, Associate Degree, some college; Health Science field preferred or related certification
Understanding of medical terminology
Experience in a large, complex, healthcare setting
Ability to effectively communicate with staff and faculty of all levels
Knowledge of University policies and procedures
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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