The primary responsiblity of the Clinical Trials Assistant is to provide needed support to the Clinical Trial Coordinators to ensure that speciment processing as well as shipping and data study requirements are carried out per protocol.
Responsibilities:Maintains departmental inventory.
Receives, processes, and ships samples per protocol
Assists with research and FDA audits as well as monitoring visits.
Assist clinical trial coordinators with study protocols.
Qualifications:High school degree or equivalent. Experience in healthare data management and/or clinical trials. Knowledge of medical terminology; analytical and organizational skills. Computer savvy. Handling of biologial specimens may be required for some trials.