Sr. Clinical Sas Analyst Programmer, MS deg., in Pharma., or Stat., w/ 1 yr., of exp; Map, integrate raw study data to CDISC - SDTM data mapping & convert to ADaM data std.
Involve in drug dev., process from protocol through FDA submissions: (Clinical Trials Phases I-III), safety reviews, integrated safety & efficacy summary (ISS/ ISE) for FDA submissions.
Validate of domains based on SDTM & ADaM(s).
Analyze data & prod., safety & efficacy tables, figures & listings.
Use SAS progr., to generate reports & formatting data in tabular form.
Wrk on prog., testing, & doc., of stat., prog., for creating stat., tables, graphs, & listing summaries of clinical trial data using SAS BASE/MACROS/STAT/ SQL/ ODS.
Program, Dev, validate & debug SAS codes for tables, listings, graphs.
Create/ Review clinical study documents (protocol, CRF, SAP, Clinical Study Report).
Review SAS data sets created according to CDISC guidelines for electronic submissions.
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)