Senior Statistical Programmer
E
EDETEKPharmaceutical, Clinical Research
Ukraine. India. Poland. Romania. Bulgaria. United StatesFull-TimeSenior
Salary not disclosed
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Job Details
- Experience
- Minimum of 5 years
- Required Skills
- R
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
- Attention to detail
- Strong communication skills, both verbal and written
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.
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