Sr. CLINICAL DATA ANALYST, MS degree in Chemistry, Computer Science, Math, Statistics or related and 1 yr. exp.: Design, validate clinical databases as per study and testing logical checks. Design CRF forms for receiving, processing and/or tracking data. Develop CRF completion guidelines CCG's, DVG. Exp. in Database and User acceptance testing (Medidata RAVE, Phase Forward Inform, Merge). Develop and provide guidance in development of data listings for data review and cleaning activities using SAS. Perform External Vendor and SAE Reconciliations. Perform coding of the events and medications using MedDRA, WHO drug dictionary. Perform quality control audits to ensure accuracy, completeness or proper usage of clinical systems and data. Support data lock activities: planning, executing listing reviews, database audit, identifying edit check maintenance needs, managing and resolving queries, identifying remaining clinical and monitoring tasks. Skills: SAS, DVG, CRF, SAE. Must be willing to travel and/or relocate to work in unanticipated locations throughout the US. Send Resume to PVR Technologies, 144 E Dekalb Pike, Ste 100, King of Prussia, PA 19406