Senior Statistical Programmer

Essential Functions And Responsibilities

• Develop and validate SAS programs to generate SDTM, ADaM datasets, tables, listings, and figures for clinical trial data
• Collaborate with biostatisticians and data managers to understand project requirements and statistical analysis plans
• Perform data manipulation and statistical analyses using appropriate programming techniques
• Develop, review and critique programming specifications and outputs to ensure accuracy and compliance with standards
• Mentor and provide guidance to junior statistical programmers to enhance their skills and productivity
• Participate in the development and implementation of programming standards and best practices
• Contribute to regulatory submissions by preparing documentation and providing support during audits

Requirements

• Bachelor's degree in Statistics, Biostatistics, Mathematics, or a related field; Master's degree preferred
• Minimum of 5 years of experience in statistical programming within the pharmaceutical or clinical research industry
• Proficiency in SAS programming; experience with R and other statistical software is a plus
• Strong understanding of clinical trial design and regulatory requirements for statistical analysis
• Experience with data management processes and data validation techniques
• Excellent problem-solving skills and attention to detail
• Strong communication skills, both verbal and written, to effectively collaborate with cross-functional teams

Benefits

Choice of comprehensive Medical, Vision and Dental Insurance plans
Paid vacation time and sick days
Corporate holidays annually
Participation in the 401K Plan
Comprehensive perks and discount programs for AAA, wholesale, insurance, Rx, fitness, pets, entertainment, etc
Health Advocate and Employee Assistance Program

Location

This is a remote position, and we are open to candidates based in the United States, Bulgaria, Romania, Poland, India, Ukraine, Sri Lanka, Philippines.