Senior/Principal Statistical Programmer

Job responsibilities
•    Uses SAS, or other software, to develop custom programming code to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming specifications.    
•    Works to ensure that outputs meet quality standards and project requirements.
•    Performs validation programming and works with other programmers, biostatisticians, and other project team members to resolve discrepancies or any findings.

When serving as a technical subject matter expert for CDISC and other industry and regulatory requirements, provides guidance and training to the Biostatistics group and other departments on the appropriate use of CDISC Standards
•    When serving as a subject matter expert for CDISC and other industry and regulatory requirements, performs compliance reviews of project deliverables for CDISC deliverables including SDTM and ADaM specifications and datasets as well as any regulatory required documents. (i.e. DEFINE.XML)

Key SKills : CDISC , ADAM, TLF, SDTM

Perks and benefits

Undergraduate degree, preferably in a scientific or statistical discipline; in lieu of degree, an equivalent combination of education and demonstrated programming experience.
•    5 plus of extensive programming experience in SAS or other required software, preferably in a clinical trial environment as demonstrated by the ability to lead multiple complex and/or global projects with teams of statistical programmers.
•    Knowledge and experience in the use of CDISC Standards for regulatory agency requirements. Experience in submissions to a regulatory agency preferred.
•    Experience in mentoring others in clinical trial process and CDISC Standards.

Note : If interested please share your updated CV to lavanya.jeevan@syneoshealth.com