Manage and perform activities associated with clinical research protocols including consenting clinical research subjects, following all IRB guidelines for the execution of IRB approved clinical research protocols. Produce and oversee participant recruitment and retention strategies. Make decisions regarding interested participants enrollment eligibility. Partner with the GCRU to ensure study visits are done correctly and according to protocols.Keeping up to date IRB activities including the reporting of adverse events and serious adverse events. Deciding if adverse events meet criteria of serious adverse events. Writing and submitting IRB applications, addendums and annual continuing review reports. This role is responsible for the review of each participant consent form and other documents to ensure that the clinical research project is in compliance with all IRB and FDA requirements. This position is responsible for ensuring all expenses are within the approved budget for this clinical research project. This includes reviewing all expenditures and signing off on expenses related to the Vitamin D, Skin and Bone Research Laboratory and Ehlers Danlos Clinical Research Program. May involve some additional administrative responsibilities such as scheduling meetings and responding to inquiries.
Bachelors degree required
Masters in related field preferred
Prior experience working on clinical research projects
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: 3228
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