DUTIES: Lead data team for studies to create & maintain library of data collection and clinical reports to promote quality and data processing; Work as Subject Matter Experts (SMEs) for data management team from review to final database lock; Guide statistical programmers & clinical biostats in developing datasets, analyzing data, generating tables, listings and figures (TLFs) for both safety & efficacy analysis output; Lead cross-trial data analytics to support clinical trial operations; Monitor functional groups in reviewing and creating reports of clinical data using reporting tool such as Looking Glass, BOXI, R-Programming & Spotfire; Instruct clinical team in designing annotated CRFs in compliance with CDISC-CDASH standards; Manage clinical data management related documentation to ensure compliance to archival/filing Requirements using Trial Master File (TMF) and eTMF (Veeva vault tool, Wingspan, Elvis); Guide study team in using Microsoft word, Excel and PowerPoint to create templates, building graphs or charts, using pivot tables, creating unique formulas and using VLookup & HLookup. Skills: Looking Glass, BOXI, R-Programming, Spotfire, CDISC-CDASH, Veeva vault tool, Wingspan, Elvis, VLookup & HLookup. Must be willing to travel and/or relocate to work in unanticipated locations throughout the US. Send resume to PVR Technologies, 501 Allendale RD, Suite 201, King Of Prussia, PA 19406.