We are seeking a Senior Statistical Programmer to provide statistical programming and analytic support clinical studies.
This position will be responsible for SAS programming and statistical analytics for clinical studies.
Expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH; system and database expertise.
Creation and review of programming specifications.
Creation of CDISC compliant SDTM and ADaM datasets.
Familiarity with statistical analysis methods and clinical data management concepts.
Performing statistical analysis, generating analytic reports, Tables/Listings/Figures, and Ad-Hoc outputs in support Clinical Study report and exploratory analysis.
Requires a Bachelor’s or Master’s degree or equivalent in Statistics, Applied Mathematics, Computer Science or related field.
BS with 10+ years or MS with 8+ of work experience in pharmaceutical/biotech or related industry.
Oncology experience preferred.
Solid programming background and advanced SAS programming skills required.
Proven knowledge of clinical trials, CDISC standards, regulatory guidance, GCP.
Must be able to work independently as well as part of a team.
Must have good communication skill (verbal and written).