Clinical Research Coordinator Intermediate

Responsibilities

• 1. Scientific Concepts and Research Design
• 2. Ethical Participant Safety Considerations
• 3. Investigational Products Development and Regulation
• 4. Clinical Study Operations (GCPs)
• 5. Study and Site Management
• 6. Data Management and Informatics
• 7. Leadership and Professionalism
• 8. Communication and Teamwork
• In this role, you will be responsible for identifying, screening, and obtaining informed consent from potential research participants
• You will communicate with participants by email and phone for a variety of study-related purposes, including recruitment and screening, scheduling study visits, troubleshooting study-related technology, and conducting follow-up to support participant compliance and retention
• You will be responsible for maintaining participant safety, monitoring and documenting adverse events, performing study testing, and acquiring study-related data
• This role also requires maintaining data security and confidentiality and adhering to HIPAA regulations and all applicable institutional policies
• Additional responsibilities include entering research data into electronic data capture systems such as OnCore, MQUARK, SharePoint, REDCap, and MyDataHelps, as well as maintaining paper case report files when needed
• You will assist in the creation and maintenance of study materials and data collection tools
• You will follow standard operating procedures and use electronic tracking systems to monitor participant recruitment, enrollment, and retention
• You may assist in preparation of reports or materials for meetings and presentations
• You will also utilize designated study hardware to perform study testing, ensure proper handling and use of study equipment, and maintain the physical security of all study hardware and related materials

Preferred

• An understanding of medical terminology
• Experience in interviewing research participants
• High degree of comfort with smart phones, and other remote tools
• Experience using MiChart, REDCap, and OnCore helpful

Benefits

• Excellent medical, dental and vision coverage effective on your very first day
• 2:1 match on retirement savings
• Glassdoor
• 4.1
• Michigan Medicine is a health care system and academic medical center that provides medical education and more. It is a sub-organization of University of Michigan.
• Ann Arbor, Michigan, USA
• http://www.uofmhealth.org/
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Qualifications

• Bachelor's degree in Health Science or an equivalent combination of related education and experience is necessary
• 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 Professionals (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 etc. within six months of date of hire
• Minimum 3 years of directly related experience in clinical research and clinical trials is necessary
• Interest in clinical health research
• Excellent organizational skills and attention to detail
• Superb interpersonal skills - comfortable speaking with healthcare providers and patients and working independently and as a member of a research team
• Ability to communicate effectively and professionally in both verbal and written form
• Ability to communicate research study details clearly over the phone
• Demonstrated ability to learn and use new skills quickly and effectively
• An understanding of medical terminology
• Experience in interviewing research participants
• High degree of comfort with smart phones, and other remote tools
• Experience using MiChart, REDCap, and OnCore helpful
• Minimum 3 years of directly related experience in clinical research and clinical trials is necessary.

Required skills

• ACRP Certified Clinical Research Coordinator (CCRC), Clinical Research, Clinical Trials, MiChart, OnCore, REDCap, Research Participant Interviewing, SOCRA Certified Clinical Research Professional (CCRP)

Preferred skills

• An understanding of medical terminology, Experience in interviewing research participants, Experience using MiChart, REDCap, and OnCore helpful

Experience

• 3+ years