Senior Statistical Programmer

Edetek is a leader in data analytics providing innovative solutions to clients in the pharmaceutical and healthcare sectors.

• 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.

• 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.