A company is looking for a Principal Statistical Programmer FSP.
Key Responsibilities
Provide technical leadership in SAS programs for analyzing and reporting clinical trial data
Ensure compliance with company SOPs and FDA / ICH / GCP regulations
Perform quality control checks of SAS code and maintain study documents
Qualifications
MS in biostatistics or related field with 8+ years of experience, or BS with 10+ years in the pharmaceutical industry
Proven expertise in SAS language and procedures used in clinical trial reporting
R programming experience is a plus
Ability to interact across multiple functions with excellent communication skills
Adaptability to changing priorities
Programmer • Glendale, Arizona, United States