Sr. SAS Programmer, MS deg. in Sci., Chem., Stat.
or rel. & 2 years exp. : Dev.
& review mapping specf. as per SDTM (IG version 3.1.3/3.2) & ADaM (IG version 1.0/1.1).
Dev. & validate Analysis datasets as per CDISC ADaM 1.0/1.1 W/generation & validation of TLFs towards CSR & ad-hoc req.
(Safety Update, Monitoring, etc.). Dev. & validate SDTM datasets as per SDTM W/generation of custom domains for specf.
studies based on TAUG. Produce efficacy & safety summary Tables, Listings, Graphs.
Create custom SAS macros & stylesheet for SDTM & TLF studies generation.
Dev. study specf.
SDRG & ADRG for submission to FDA as per guidelines.
Dev. & review tables, listings by pooling multiple studies for DSUR submission.
Exp. on Open CDISC/ Pinnacle 21 validator to check compliance & provide justification for various Errors & Warnings generated.
Must be willing to travel and/or relocate to work in unanticipated locations throughout the US.
Send Resume to Statminds LLC., 515 Shoemaker Road, Suite 201, King of Prussia, PA, 19406
Location/Region: King Of Prussia, PA (US - 19406)