Statistical Analyst - ADaM Programming (Hybrid)

The Statistical Analyst is an integral role in the research and development of new pharmaceutical products. The primary responsibilities for this role include the analysis and reporting of clinical trial data without supervision for routine activities and with supervision for more complex activities. The Statistical Analyst interfaces with Statistics, Clinical Data Strategy & Operations and Development Operations.
Responsibilities:
Leads the statistical programming activities for routine studies.
Create documentation for regulatory filings including reviewers guides and data definition documents
Participate in the development of standard SAS Macros, as well as, presenting information on existing Macros
Produce dynamic and static data visualizations to communicate quantitative analyses.
Develop SAS programs for the creation of ADaM data sets following CDISC standards.
Develop SAS programs for the creation of Tables, Listings and Figures.
Validation of ADaM data sets. Validation of Tables, Listings and Figures.
Create specifications for the structure of ADaM data sets for individual studies and integrated data
Minimum Qualifications:
MS in Statistics, Computer Science or a related field with 2+ years of relevant experience. OR BS in Statistics, Computer Science or a related field with 4+ years of relevant experience.
Experience in pharmaceutical clinical trials
Demonstrated practical understanding of SAS programming related to drug development.
Experience creating and reviewing ADaM datasets for analysis
Preferred Qualifications:
Demonstrated ability to support efficacy analyses across clinical development phases and therapeutic areas.
Other Required Skills:
Ability to communicate clearly both oral and written.
Basic understanding of CDISC Standards.
Basic understanding of the drug development process.

Skills
Documentation

Experience
4+ yrs

Employment type
Full-time

Work arrangement
Hybrid