The Clinical Research Coordinator II (CRC) performs increasingly complex tasks to facilitate clinical research, while providing service to Virginia Mason Physicians on their clinical trials specializing in Cardiology, Asthma/Allergy, Rheumatology, and Neurology.
• New study preparation
• The creation of study budgets
• Subject screening and recruitment
• Informed consent
• Subject history
• Adverse events
• Concomitant medication review
• Regulatory document filing
• Preparation for study monitor visits
• Test article (ta) handling
• Completion of case report forms
• Maintenance of source documents
• Proper standard or research billing
• Ensuring site quality
Subject care requirements may include appointment scheduling, records review, treatment coordination, collecting vital signs, subject health assessment, and telephone triage/screening. The CRC may also perform phlebotomy, specimen processing and participate in process improvement events as necessary.
• Requires 2 years of experience
• Certification preferred
• Requires some higher education or vocational training specializing in healthcare
• May require CPR certification or other specialized training
• A healthcare assistant certificate may also be required
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, citizenship, disability or protected veteran status.