The Statistical Programmer I is responsible for providing programming support for clinical trials.

Responsibilities:

• • Understand and implement CDISC and other regulatory standards
  • Follow internal SAS programming conventions
  • Apply knowledge of SAS programming to program and/or validate statistical outputs according to the statistical analysis plan and other specifications; including but not limited to:
    
    • SDTM, ADaM or other derived datasets
    • Tables, listings and figures
  • Review and provide input on case report form design
  • May draft programming specifications
  • Work effectively with other programmers, statisticians, data managers, database programmers and other cross-functional team members to ensure accurate and high-quality statistical outputs
  • Standard Operating Procedures (SOPs)
    • Strong understanding of departmental and company procedures; ability to guide others on procedures
  • Additional Responsibilities
    
    • Perform other duties as requested by management

Qualifications:

• The ideal candidate should have a degree in Statistics, Computer Science, or a closely related field or equivalent of education and experience.
• At least 1 year of direct SAS programming experience in pharmaceutical development or CRO environment preferred, but not required.
• Excellent oral and written communication skills, organizational skills, and attention to detail are required