Clinical Trial Coordinator, School of Medicine, Arthritis Center/Rheumatology

Boston University
BOSTON, Massachusetts, United States
08 Jun 2018
End of advertisement period
06 Jul 2018
Contract Type
Full Time

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.

Required Skills

 1-3 years of experience and Bachelor’s degree required. Responsible for all aspects of the management and conduct of multiple study protocols. Attended investigator meetings, site qualification, selection, and initiation meetings, staff training and presentations on study protocols and procedures. Conducts trial start up and initiation, as well as IRB and WIRB regulatory submissions, development of specific source documents and CRF completion and query resolution. Schedule and assist with site monitoring visits as well as protocol amendments and continuing reviews, as well as day-to-day operations including patient visits, scheduling, and assessments. Assist in study close out, study file storage, drug and device return, and documentation.

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.