The primary purpose is to coordinate and implement clinical trials and clinical research projects, documentation, protocol education, research sample storage, patient recruitment and patient assessment within Boston University Arthritis Center.
Initiation of trials: Attend investigator meetings, site qualification and site initiation meetings regarding anticipated study protocol.
Implementation of trials: Assist with IRB submissions, complete and submit required regulatory documents, develop source documentation.
Administration: Assist with chart review, subject recruitment, scheduling of subject visits and completion of subject assessments. Interact with ancillary service departments such as Pulmonary Function, Radiology and the General Clinical Research Unit. Complete requisitions and ensure forms, tests and procedures are conducted per study protocol. Complete data entry using study specific EDC system. Accommodate and help facilitate monitoring visits as needed. Assist in study close out, file storage, drug and device return and documentation. Ensure research activities comply with institutional and federal guidelines. Adhere to Human Subjects Protection and Good Clinical Practice ICH Guidelines and maintain required training certifications.
Bachelor's degree and 1-3 years of experience 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.
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