Senior Statistical Programmer

Responsibilities :

• Hands-on statistical programming to support CSR, publications, presentations, DSUR, IB update, safety data review, reconciliation, ad hoc analyses, patient profiles, and monthly safety reports in a fast-paced environment.
• Write or review data specifications for Study Data Tabulation Model (SDTM) and Analysis Data Model (ADaM).
• Validate and create SDTM, ADaM, and Tables, Figures, and Listings (TFLs), including associated documentation like define.xml using SAS.
• Ensure that all programming and data are conducted in compliance with GCP, relevant SOPs, and regulatory requirements.
• Assist in the development of template programs or macros and standard specifications to improve efficiency in the Statistical Programming group.
• Work on multiple tasks at same time and prioritizes tasks to meet timelines on a regular basis.
• Collaborates with Biostatisticians, Clinical Data Management, and Clinical Research Scientists on studies when needed.
• Support RWE data curation and summaries in coordination with Biostatistics.
• May assist with testing R and relevant R packages to either validate or develop R-based code solutions.

Requirements :

7+ years of statistical programming experience in the pharmaceutical industry.

Strong SAS programming and statistical background along with experience with Base SAS, SAS Macros, SAS / STAT, SAS / Graph, SAS / SQL, SAS / ODS.