Work with assessment, design and/or implementation of data standards (e.g., CDISC SDTM & CDASH).

Responsible for drafting, uploading, and reviewing study specific documents such protocol, statistical analysis plan.

Develop global SAS macros to improve efficiency of pharmacokinetic and pharmacodynamic analyses.

Annotate case report forms (CRFs) according to CDISC Implementation Guideline for migration to SDTM.

Design and develop project-specific SAS programs for biostatisticians, often producing analysis datasets, reports, or graphics.

Follow established standardized design & programming procedures (CDISC).

Follow standardized SDTM migration programming procedures to create quality Standard Data Tabulation Model (SDTM) compliant SAS datasets & Define.XML documents.

Create statistical analysis outputs in support of final reports, abstracts, posters, manuscripts, & clinical publications.

Position Requirements: Bachelor's degree or a foreign equivalent degree in Healthcare Informatics, Health Admin, Pharmacology, Toxicology, Pharmacy, Chemistry, Computer science, Public Health, Bio Informatics, Bio Technology, Statistics or related plus two years of work experience in any position/title providing experience with SAS.

Special Skills: Qualifying experience must include experience with SAS. Position requires travel/relocation to various unanticipated client locations throughout the U.S. with expenses paid by the employer.

Benefits: Medical, Life Insurance and 401K.

Standard Company Benefits.