Contract Senior Statistical Programmer (Remote)

The Senior Statistical Programmer will be expected to have hands-on skills and experiences in production or validation of CDISC SDTM, ADaM datasets, and Tables, Listings, Figures to support clinical study reports, ISS, or ISE for assigned projects with minimal supervision. Independently provide programming supports to statisticians in planned or adhoc analysis, and demonstrate SAS programming proficiency. This position requires a comprehensive knowledge of CDISC standards, clinical trial study design, and electronic data submission requirements. Work collaboratively with study team to meet study deliverables and timeline for statistical data analysis and reporting.

Other responsibilities include but not limit to: develop and maintain standard programs, macros, templates, and libraries for use in clinical studies.

Key Responsibilities

• Participate study team meeting to represent the Statistical Programming function to support or lead the study,, focusing on data integrity, collaboration and on-time deliverables.
• Has sufficient understanding to follow an analysis plan and standard study SDTM, ADaM data specification and provide programming support for all of required deliverables.
• Process clinical data required for statistical analysis. Develop SAS code or macros for preparing, processing and analyzing clinical data.
• Interact with members of project teams, statistician and data management personnel to perform statistical programming activities.
• Provide support in production or validation of summary tables, data listings and graphs required for trial report and clinical development, and CDISC data sets for regulatory submission.

Do you have experience in SAS language?, Do you have a Bachelor’s degree?, * A bachelor’s degree in statistics, mathematics or equivalent with at least 8 years experience in pharmaceutical or bio-pharmaceutical industry, a master’s degree or PhD in statistics or computer science is preferred.

• Demonstrated good verbal, written communication skills and interpersonal skills.
• Self-motivated, with initiative and the ability to take ownership of, and follow through with, specific tasks.
• Ability to multi-task and shift priorities quickly while working under tight deadlines.
• Experience in data analysis of real-world data is plus. Sufficient programming skill with R is preferred., * Pharmaceutical SAS programming: 8 years (Required)