Senior Statistical Programmer

Responsibilities

• ▹Develop and validate SAS programs to generate SDTM and 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 guide junior statistical programmers
• ▹Participate in developing and implementing programming standards and best practices
• ▹Contribute to regulatory submissions by preparing documentation and supporting audits

Requirements

• ▹Bachelor's degree in Statistics, Biostatistics, Mathematics or a related field; Master's degree preferred
• ▹Minimum of 5 years of statistical programming experience in the pharmaceutical or clinical research industry
• ▹Proficiency in SAS programming
• ▹Strong understanding of clinical trial design and regulatory requirements for statistical analysis
• ▹Experience with data management processes and data validation techniques

Nice to have

• ▹Experience with R and other statistical software

Soft skills

What we offer

• ▹Remote position open to candidates based in the United States, Bulgaria, Romania, Poland, India, Ukraine, Sri Lanka and the Philippines
• ▹Benefits vary by country but remain competitive; for U.S. employees: medical, vision and dental insurance, paid vacation and sick days, corporate holidays, 401K plan, perks and discount programs, Employee Assistance Program

About the company

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