Clinical Research Coord Assoc

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 Brighton Center for Specialty Care, providing study coordination support to faculty and research teams for the University of Michigan Rogel Cancer Center – an NCI‑Designated Comprehensive Cancer Center and a member of the National Comprehensive Cancer Network (NCCN). The Oncology CTSU is a diverse team of 150 clinical research professionals dedicated to moving this mission forward through cutting‑edge early phase trials to practice‑changing phase III trials. As a team member, you will receive education, training, career development, and certification support, and you will have specialized roles and growth opportunities tailored to your career path. Responsibilities Independent knowledge, skills, and abilities within all eight competency domains are expected: Scientific Concepts and Research Design Ethical Participant Safety Considerations Investigational Products Development and Regulation Clinical Study Operations (GCPs) Study and Site Management Data Management and Informatics Leadership and Professionalism Communication and Teamwork Given the complex nature of oncology trials, the coordinator specializes in clinic coordination and may occasionally work at the Ann Arbor location for training or support. Typical duties include: Clinical Research Coordinator – Associate Understand and execute protocol elements and study procedures. Anticipate and mitigate potential protocol non‑compliance. Interpret study requirements and ensure compliance. Accurately implement protocol procedures. Perform non‑GCP related study management activities. Perform study procedures with minimal supervision. Triage simple subject issues appropriately. Maintain specimen integrity: collection, processing, packing/shipping, storing, labeling, tracking. Operate basic clinical lab equipment—centrifuge, freezers, pipettes, and adhere to safety guidelines. Explain CTSU's role in initiating new studies and subject visit billing. Process research samples. Clinical Research Coordinator – Technician Provide coordination for simple and moderately complex studies; support a portfolio of projects. Perform moderately complex study procedures accurately. Triage simple subject concerns. Assess studies, troubleshoot implementation issues. Collect simple to moderately complex data during visits. Reconcile financial accounts for study participants with CTSUs. Assist with local quality control efforts. Process research samples. Clinical Research Assistant Assist with multiple clinical research studies; perform tasks with consistency and accuracy. Navigate resources and tools effectively and identify support when needed. Escalate issues appropriately when additional intervention is required. Required Qualifications Clinical Research Coordinator – Associate Bachelor’s Degree in Health Science or equivalent education and clinical research experience. Certification as Certified Clinical Research Coordinator (CCRC) through ACRP or Certified Clinical Research Professional (CCRP) through SoCRA, or equivalent. Clinical Research Coordinator – Technician Associate Degree in Health Science or equivalent education and experience. 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, or Foreign MD. Minimum 3 years of human subject experience in clinical, laboratory, or health regulations settings. Clinical Research Assistant High School Diploma or GED. Desired Qualifications Clinical Research Coordinator – Associate 4+ years of direct related experience. Clinical Research Coordinator – Technician Bachelor’s Degree, Health Science field preferred or related certification. Understanding of medical terminology. Experience in a large, complex healthcare setting. Effective communication with staff and faculty at all levels. Knowledge of University policies and procedures. Clinical Research Assistant Bachelor’s Degree, Health Science field preferred or related certification. Understanding of medical terminology. Experience in a large, complex healthcare setting. Effective communication with staff and faculty at all levels. Knowledge of University policies and procedures. Why Join Michigan Medicine? Michigan Medicine is one of the largest health care complexes in the world, with a history of groundbreaking medical and technological advancements. It employs over 30,000 staff and is committed to attracting, inspiring, and developing outstanding people in medicine, science, and healthcare. Working here contributes to advancing a world‑class academic health system and to making a broader impact on patient care and research. What Benefits can you Look Forward to? Excellent medical, dental, and vision coverage effective on your first day. 2:1 match on retirement savings. Modes of Work Positions eligible for hybrid or mobile/remote work modes are at the discretion of the hiring department. Work agreements are reviewed annually and may change at any time. Work Schedule Monday through Friday, core business hours with potential evening or weekend work to meet deadlines or support patient care. Underfill Statement This position may be underfilled at the CRC‑Technician or Clinical Research Assistant title based on selected candidates’ qualifications. Additional Information Michigan Medicine is committed to advancing inclusion, diversity, equity, accessibility, and belonging. The community supports a diverse workforce and fosters a respectful and safe work culture. Background screening and pre‑employment drug testing are performed in compliance with applicable law. Selected candidates will undergo these assessments upon acceptance of a contingent job offer. U‑M EEO Statement The University of Michigan is an Equal Opportunity Employer. It is committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants, including protected veterans and individuals with disabilities. #J-18808-Ljbffr University Of Michigan