Corewell Health·Royal Oak, Michigan
The Clinical Research Coordinator II is responsible for protocol coordination, including subject recruitment, enrollment, and implementation of research protocols. They also function as a regulatory specialist or auditor to ensure compliance with institutional policies and federal regulations.
Royal Oak - Full time, day shift About Corewell Health William Beaumont University Hospital (Royal Oak) Corewell Health William Beaumont University Hospital opened on Jan.
24, 1955 as a 238-bed community hospital.
Today, the hospital is a 1,101-bed major academic and referral center with Level I adult trauma and Level II pediatric trauma designations.
Corewell Health William Beaumont University Hospital has 43 residency and fellowship programs with 454 residents and fellows.
Corewell is the exclusive clinical partner of the Oakland University William Beaumont School of Medicine, with more than 1,400 doctors on faculty.
Scope of Work May function as study personnel, regulatory specialist or auditor.
The CRC II study personnel is responsible for protocol coordination, including subject recruitment, enrollment, implementation, and follow-up of appropriate research protocols.
The CRCII study personnel promotes good clinical practice in the conduct of clinical investigations by possessing knowledge of federal regulations and guidance documents for the conduct of clinical trials and human subject protection.
The CRC II Regulatory Specialist comprehensively coordinates all processes related to HIC business in order to insure compliance with institutional policies and federal regulations governing human subject research.
The CRC II Auditor provides ongoing review of all patient and regulatory materials based on Good Clinical Practices.
The CRC II Auditor evaluates accuracy and completeness of documents per regulatory, institutional and study specific requirements.
The Auditor's activities will include but are not limited to, review of subject eligibility and screening procedures, review of subject research visits and data collection and review of CRF's, source documents and other essential documents.
Required Bachelor's Degree or equivalent in a health-related field, two or more years of clinical research experience, and National Research Certification within six months of hire OR five or more years of clinical research experience, and National Research Certification, OR clinical specialist with technician registration or therapist licensure (e.g., Radiation Therapist, Cardiovascular Specialist) and National Research Certification within six months of eligibility. Previous Cardiology Research experience highly preferred Must have good working knowledge of all applicable FDA guidelines and Good Clinical Practices. Required CRT-At least one Certification from preferred list - UNKNOWN Unknown Upon Hire preferred CRT-Clinical Research Professional, Certified (CCRP) - SOCRA Society of Clinical Research Associates Upon Hire preferred Or CRT-Clinical Research Coordinator, Certified (CCRC) - ACRP Association of Clinical Research Professionals Upon Hire preferred Or CRT-IRB Professional, Certified (CIP) - UNKNOWN Unknown Upon Hire preferred CRT-Basic Life Support (BLS) - AHA American Heart Association Upon Hire preferred Or CRT-Basic Life Support (BLS) - ARC American Red Cross Upon Hire preferred
Candidates must hold a bachelor's degree in a health-related field and possess at least two years of clinical research experience. National Research Certification is required within six months of hire, and a working knowledge of FDA guidelines and Good Clinical Practices is essential.
Market context
Clinical Research Coordinator II positions in Michigan are typically driven by hospitals, universities, and research centers running ongoing studies. This role is competitive because employers often prefer candidates with medical or science experience and clinical research certification, while a bachelor’s degree or equivalent experience is required. Review the AI-summarized requirements and benefits on this page to save time, and tailor your application to show study coordination, compliance, and patient-facing experience.
