Clinical Research Coord Assoc

Apply Now How to Apply A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position. Job Summary This position will serve as a Clinical Research Coordinator Associate (or Clinical Research Coordinator Technician) 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). We are among the top‑ranked national programs in research and patient care with members holding $120M in annual direct research funding. Our mission is to reduce the cancer burden and improve cancer outcomes through research, innovation, and transdisciplinary collaboration. With the Oncology CTSU, you will join a diverse team of 150 clinical research professionals dedicated in moving this mission forward through cutting‑edge early phase trials to practice‑changing phase III. As a team member, we will invest in your education, training, career development and certification. We also offer a variety of specialized roles and growth opportunities to fit your desired career path and goals. Benefits Excellent medical, dental and vision coverage effective on your very first day 2:1 Match on retirement savings Responsibilities Characteristic Duties And Responsibilities 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 Examples of duties a successful candidate in this role will perform: Clinical Research Coordinator – Associate Demonstrates understanding of protocol elements/requirements and 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. Clinical Research Coordinator – Technician 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. Required Qualifications Clinical Research Coordinator – Associate 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 Professional (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 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. Clinical Research Coordinator – Technician Associate Degree in Health Science or an equivalent combination of related education and experience is necessary. ONE of the following: 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 qualifying experience prior to applying. 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. 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. 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. Ability to effectively communicate with staff and faculty of all levels. Knowledge of University policies and procedures. Work Schedule Monday through Friday, core business hours. Occasionally evening or weekend work to meet deadlines or support patient care. This position is located at Brighton (BCSC). May have to come to Ann Arbor location for training or to provide help/coverage when needed. U‑M EEO Statement The University of Michigan is an equal employment opportunity employer. #J-18808-Ljbffr