Clinical Trials Assistant I - Kelly Services
CurrentCollect and document data from qualified subjects participating in one of 5-6 key clinical research studies.Conduct personal structured interviews within specified protocol windows. Track and seek out multiple sources, including study coordinators, for difficult-to-locate subjects to maximize study participation during follow-phases of key clinical trial studies.Perform selected data entry of Summaries following personal structured interviews noting any significant subject characteristics relevant to studies according to protocol timelines.Identify and report data quality and quantity problems to Study Coordinators through review and analysis of standard computer reports, logs and protocol timelines, remaining alert for database problems, particularly on new studies.