Statistical Programmer

Description:

The incumbent is responsible for the quality, as well as the timely and efficient delivery of project statistical programming outputs. This role performs supports statistical programming activities for studies and programs in the Biometrics team.

Key Role And Responsibilities
 

• Accountable for quality, timely and efficient delivery of statistical programming work
• Develops and validates datasets, TLFs, and adhoc analyses for in-house deliverables.
• Develops and validates standard department-level programs and templates.
• Participates in the development of best practices, standards and process improvement initiatives.
• Maintains expertise of the latest industry and regulatory requirements to stay current.
   

Skills

REQUIRED Qualification:
 

• 3+ years within the pharmaceutical, biotechnology or clinical research industry.
• Proven experience using statistical software packages SAS and R.
• Strong understanding of statistical analysis methodologies and criteria.
• Proficiency in CDISC SDTM and ADaM standards.
• Experience with validation tools Pinnacle 21 or CDISC CORE
• Prior experience in the analysis of hematology or oncology clinical trial data.