Available Positions


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.

REQUIREMENTS: Master’s degree in Computer Science, Computer Information Systems with 2 years of experience in a job title with similar duties and skills.

SALARY: $105, 144.00/Year

HOURS: 40 hours/week, Mon- Fri, 9:00am – 5:00pm

JOB LOCATION: PVR Technologies, 501 Allendale RD, Suite 201, King of Prussia, PA 19406

CONTACT: Holly Cox, HR Associate

PHONE: 610-337-1935