The Amyloidosis Center is looking a Clinical Research Coordinator to work on one or more international multi-center clinical trials. The Clinical Research Coordinator will perform research and administrative tasks including but not limited to study subject recruitment, assessing study eligibility, scheduling evaluations, coordinating research assessments by ophthalmology, cardiology, and neurology services, entering results on various electronic data capture websites, monitoring subject response to investigational treatments, and interacting with subjects enrolled in an international multi-center clinical trial. Will conduct specific neurologic and exercise tests on subjects per study protocol, maintain study regulatory documents, submit adverse event documents and IRB reports, and maintain subject records. Will also support IRB submissions. Duties will include developing budgets, monitoring financial accounts, arranging travel and lodging for subjects as necessary, and generating invoices for travel reimbursement of participants and vendors for services rendered.
Required Skills Highly organized person with a Bachelors Degree and 1-3 years experience working in clinical research. Experience as a coordinator in a medical or social science field helpful. Experience with study start-up and IRB submissions a plus. Microsoft Office skills required.
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. We are a VEVRAA Federal Contractor.
Internal Number: 8972
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