Clinical Research Coordinator/Program Manager
Current• Act as an effective liaison between research regulatory departments• Develop successful action plans if needed for regulatory audit findings• Provide valuable regulatory compliance advice to SFVAMC principal investigator • Assist SFVAMC principal investigator with research protocol modifications, additions, and submissions• Recruits and randomizes patients into studies• Works closely with the site clinical staff and uses good clinical judgement • Schedules follow-up visits, collects data on study patients outlined in the study protocol• Reports on and carries out data analysis tasks (including but not limited to data reports, tables, and graphs) related to ongoing and developing research studies • Maintains a complete study file of data forms for each patient• Assists the Site Investigator in preparation of the documents required for the IRB and R&D Committee approvals • Consistently communicates with patient and staff throughout the work environment in a courteous, tactful, and helpful manner• Handles routine correspondence including using word processing programs, copying and faxing of letters, memorandum, requests for supplies and equipment, etc