SAS Programmer / Clinical

SAS PROGRAMMER / CLINICAL 100% Remote. Required Skills:

• 6+yrs of SAS programming experience in biopharma setting supporting Phase 1-4 clinical trials in CRO or pharmaceutical industry.
• Solid CDISC Standards knowledge, 4+ years of ADaM programming experience supporting safety and efficacy analysis.
• Well experienced in converting information from aCRF, SDTM data, SAP into ADaM specifications and review TLF outputs from vendors.
• Experience on creating Tables, Listing and Figures for clinical study report using proc report or data null.
• Knowledge of regulatory submission process, experience on creating ISS, ISE ADaM datasets and TLFs is a plus.
• Team player with excellent communication skills and experience working with statistical programmers, statisticians, and data management personnel.
• Expertise in Oncology programming, SAS certification, leading studies, ISS, ISE, submission, etc.,
• Team player
• Late phase Oncology
• Good team player who can work independently with minimal guidance.
• Enterprise Guide experience is a plus.