A company is looking for a Principal Statistical Programmer FSP.
Key Responsibilities :
Provide technical leadership in SAS programming for analyzing and reporting clinical trial data
Ensure compliance with company SOPs and FDA / ICH / GCP regulations
Perform quality control checks and maintain study documents per standard process
Qualifications :
MS in biostatistics or related field with 8+ years of experience, or BS with 10+ years of experience in the pharmaceutical industry
Proven expertise in SAS programming and clinical trial reporting
R programming experience is a plus
Experience in providing technical leadership and conducting briefings
Ability to adapt to changing priorities
Programmer • Fort Lauderdale, Florida, United States