Clinical Research Coord Inter

Job Summary Clinical research coordinator (CRC) provides study coordination and/or project management for multiple clinical research studies of any complexity. The role requires mastery of the Michigan Medicine CRC Career Ladder, oversight of clinical research projects, and independent decision‑making on matters within scope. The coordinator serves on the Pediatric Critical Care Medicine Division at the University of Michigan C.S. Mott Children’s Hospital, supporting study coordination, specimen collection, and data management. Key Responsibilities Screen, recruit, consent, and monitor research participants in accordance with study protocols Coordinate study visits and follow‑up activities Collect, process, store, ship, and track research specimens, ensuring integrity and compliance with protocol and regulatory requirements Maintain accurate source documentation and study data; perform quality assurance/quality control activities Collaborate with multidisciplinary teams including clinicians, nurses, research pharmacy, and administrative staff to ensure protocol adherence and resolve issues Identify and troubleshoot study‑related, participant, and workflow challenges Report and route adverse events (AEs/SAEs) in accordance with institutional, sponsor, and regulatory requirements Support multiple concurrent studies, prioritizing tasks and timelines effectively Assist with IRB regulatory processes including study start‑up, amendments, continuing reviews, and safety reporting Communicate with sponsors and CTSU regarding study progress, recruitment, and operational considerations Serve as a liaison between study teams, sponsors, IRB, and regulatory agencies Participate in investigator and scientific meetings as needed Supervision Reports to the Clinical Research Project Manager and works closely with the Division Research Director. This position manages a portfolio of multi‑site clinical research as assigned. Required Qualifications Excellent interpersonal, verbal, and written communication skills with strong attention to detail Proficiency in Microsoft Office applications Excellent organizational skills, including the ability to multitask and work well under time constraints and deadlines Willingness to be flexible in a dynamic working environment Ability to work independently with minimal supervision and collaborate effectively with diverse teams Experience with REDCap is required Bachelor's Degree in Health Science or an equivalent combination of related education and experience (minimum 3 years of directly related experience for Intermediate, 2 years for Associate, 1 year for Technician) Certification as a Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) from ACRP or SOCRA, obtained or completed within six months of hire Desired Qualifications 6+ years of directly related experience for Intermediate, 4+ years for Associate Bachelor’s degree in Health Science or equivalent desirable for Technician Understanding of medical terminology, experience in a large complex health care setting, effective communication with staff and faculty, and knowledge of university policies and procedures Benefits Excellent medical, dental and vision coverage effective on the first day 2:1 match on retirement savings EEO Statement The University of Michigan is an equal employment opportunity employer. #J-18808-Ljbffr