Michigan Medicine · 16 hours ago
Clinical Research Coordinator Associate/Technician/ Assistant- Term limited
Ann Arbor, MI
Full-time
Onsite
Entry, Mid Level
1+ years expMichigan Medicine is seeking a Clinical Research Coordinator Associate/Technician/Assistant to support clinical research studies within the Department of Anesthesiology, Chronic Pain and Fatigue Research Center. This role involves coordinating study activities, ensuring compliance with protocols, and interacting with study participants. The candidate will work on a range of clinical research studies and must demonstrate strong organizational and communication skills.
EducationHealth CareMedical
Responsibilities
Experience as part of a team with all 8 competency domains is expected
Participant Screening and Recruitment
Explaining study thoroughly, reviewing informed consent, answering any questions, following GCP/IRB and obtaining consent
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
Demonstrates the ability to document data in accordance with ALCOA-C principles
Describes protocol structure and explains how to interpret study requirements to ensure study compliance
Demonstrates accurate implementation of protocol procedures
Explains and performs study related management activities
Performs study procedures with minimal supervision
Triages subject issues appropriately
Schedules and runs study visits with complex data collection
Perform Quantitative Sensory Testing (QST) inside and outside of MRI, and willingness to be trained
Preparation datasheets, questionnaires, study related documents
Tracking and communication with study subjects
Complete subject documentation and follow up
Assist with data entry and capture
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
Submit Human Subjects Incentive Program (HSIP) requests
Assist with eResearch submissions
Travel to the North Campus MRI for study visits or Research Pharmacy
Performs moderately complex study procedures with accuracy
Assesses studies for execution and troubleshoots potential implementation issues
Completes simple to moderately complex data collection during study visits
Assists with local quality control efforts
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 an equivalent combination of related education and experience is necessary
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
Minimum 2 years of directly related experience in clinical research and clinical trials is necessary
Attention to detail and accuracy
Excellent attendance and strong work ethic in past settings
Excellent interpersonal skills
Demonstrated ability to prioritize and exercise good judgement
Associate degree in health science or an equivalent combination of related education and experience is necessary
Minimum 1 year directly related experience in clinical research and clinical trials is necessary or an advanced degree in a health-related area 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
High School Diploma
Attention to detail and accuracy
Excellent attendance and strong work ethic in past settings
Excellent interpersonal skills
Preferred
4+ years of direct related experience
Phlebotomy experience
Lab processing experience
Experience with eResearch
Pediatric research experience
Bachelors Degree in Health Science or an equivalent combination of related education and experience is desirable
Associate degree or equivalent combination of education and experience; Health Science is preferred
Benefits
Human Subjects Incentive Program (HSIP)
Background Screening
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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