Michigan Medicine
Clinical Research Coord Assoc/Technician/Assistant
Michigan Medicine, Ann Arbor, Michigan, us, 48113
Clinical Research Coordinator Associate/Technician/Assistant
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Clinical Research Coordinator Associate/Technician/Assistant
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Michigan Medicine
Job Summary This position will serve as a Clinical Research Coordinator Associate in the Oncology Clinical Trial Support Unit (O-CTSU) – Clinic Research Group located in the Rogel Cancer Center. The role provides administrative study coordination and data entry support to faculty and research teams.
Key Responsibilities
Demonstrates understanding of protocol elements and executes study procedures with minimal supervision.
Anticipates and mitigates potential protocol non‑compliance and performs non‑GCP related study management activities.
Ensures integrity of specimen management (collection, processing, packing/shipping, labeling, tracking).
Triages simple subject issues appropriately and actively uses EMR and databases (OnCore, CTMS, EDC).
Collaborates with CTSUs to reconcile financial accounts and assist with local quality control efforts.
Qualifications – Associate
Bachelor’s Degree in Health Science or equivalent education and clinical research experience.
Certified Clinical Research Coordinator (ACRP/CCRC) or equivalent SOCRA/CCRP certification, completed or passed within six months of hire.
Minimum 2 years of directly related experience in clinical research and clinical trials.
Qualifications – Technician
Associate degree in Health Science or equivalent combination of related education and experience.
Minimum 1 year of directly related experience in clinical research and clinical trials.
Qualifications – Assistant
High School Diploma or GED.
Benefits
Excellent medical, dental, and vision coverage effective on the first day.
2:1 match on retirement savings.
Work Schedule Monday through Friday, core business hours. Occasionally evening or weekend work to meet deadlines or support patient care.
EEO Statement The University of Michigan is an equal employment opportunity employer.
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Clinical Research Coordinator Associate/Technician/Assistant
role at
Michigan Medicine
Job Summary This position will serve as a Clinical Research Coordinator Associate in the Oncology Clinical Trial Support Unit (O-CTSU) – Clinic Research Group located in the Rogel Cancer Center. The role provides administrative study coordination and data entry support to faculty and research teams.
Key Responsibilities
Demonstrates understanding of protocol elements and executes study procedures with minimal supervision.
Anticipates and mitigates potential protocol non‑compliance and performs non‑GCP related study management activities.
Ensures integrity of specimen management (collection, processing, packing/shipping, labeling, tracking).
Triages simple subject issues appropriately and actively uses EMR and databases (OnCore, CTMS, EDC).
Collaborates with CTSUs to reconcile financial accounts and assist with local quality control efforts.
Qualifications – Associate
Bachelor’s Degree in Health Science or equivalent education and clinical research experience.
Certified Clinical Research Coordinator (ACRP/CCRC) or equivalent SOCRA/CCRP certification, completed or passed within six months of hire.
Minimum 2 years of directly related experience in clinical research and clinical trials.
Qualifications – Technician
Associate degree in Health Science or equivalent combination of related education and experience.
Minimum 1 year of directly related experience in clinical research and clinical trials.
Qualifications – Assistant
High School Diploma or GED.
Benefits
Excellent medical, dental, and vision coverage effective on the first day.
2:1 match on retirement savings.
Work Schedule Monday through Friday, core business hours. Occasionally evening or weekend work to meet deadlines or support patient care.
EEO Statement The University of Michigan is an equal employment opportunity employer.
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