Description
Clinical SAS Programmer12 month Contract
A Major CRO
RTP, North Carolina
Start ASAP
Job Description
Clinical SAS Programmer
Tasks and Responsibilities:
Build programming specifications for safety and efficacy analysis database based on the Statistical Analysis Plan and report specifications (development of CDISC ADaM and SDTM)
Generate analysis datasets, tables, listings and figures to support writing of Clinical Study Reports and other regulatory filings
Generate all necessary output for the compilation of statistical appendices for reports (e.g. Annual Safety Reports, Clinical Study Reports, Statistical Reports, etc)
Perform verifications of analysis datasets and tables, listings and figures created by another team member
Complete programming projects on time and with the best quality control.
Review and provide feedback on CRFs and edit specifications
Requirements:
Proficiency in SAS BASE, SAS STAT, SAS/GRAPH, SAS Macros, PROC SQL, and CDISC standard
Strong programming experience in clinical trials with experience in CDISC SDTM and ADaM data set generation
Skills to be a good and motivated communicator, organized and proactive in pursuing and performing duties in a team atmosphere.
Statistics degree is a plus
Experience:
5+ years Clinical SAS experience with clinical trials.
Must have strong submissions experience.
Good understanding of CDISC, SDTM and ADAM standards. Good leadership experience and a solid work history preferred and not a lot of positions held in a short period of time.
APPLY NOW, email your resume to me or call for more details.
Thanks
Paul Dai
To find out more about Real please visit www.realstaffing.com