Duties and Responsibilities:

Duties include but are not limited to:

Support CRC to meet industry trial data deadlinesObtain source documentation for patients enrolled onto clinical trialsAssist CRC with case report form completionAssist CRC with query resolutionAssist in SAE reporting and trackingCreate and maintain patient visit tracking spreadsheets for CRCMaintain and archive study administrative fileMaintain and archive regulatory filesAssist in ensuring source document templates are accurateAttends meetings as assigned and reports on actionsParticipates in educational activities and programsMaintains strictest confidentialityWorks closely and effectively with all other department colleaguesAssists other staff as requested and performs other related work as needed.Assigned special procedural projects to enhance the functioning of the research programThroughout the conduct of the trial, assesses adherence to company SOPs, Good Clinical Practice (GCP), and FDA regulations.All other duties as assigned