Job description

• Analyze and develop Statistical models/programs for clinical studies using SAS, Phase I-IV Clinical Trial domain, CDISC SDTM & ADAM Standards
• Analyze and coordinate SAS programming activities supporting ISS/ISE TFL’s using Statistical Analysis, STAT Model/Program Development and Validation
• Deploy data models, graph-based algorithms for TLGs reporting and CRT Submission
• Maintain study databases and release updated SAS graphs datasets for statistical/Data analysis
• Create data listings, summary statistical tables and ad-hoc reports for clinical trial data

Requirements

Must have a Master’s Degree in Applied Statistics, Pharmaceutical Management, or BioStatistics plus 2 years experience in job offered. Require skills and knowledge in SAS, Phase I-IV Clinical Trial domain, CDISC SDTM & ADAM, ISS/ISE, CRT Submission, Statistical Analysis, STAT Model/Program Development & Validation, TLGs. Allow telecommuting. Required 100% travel to unanticipated client locations in USA.