Senior Statistical Programmer

Responsibilities:Implement CSDIC standards and guidelines for data management and analysis in clinical trials.Transform and map raw clinical trial data to SDTM and ADaM datasets.Collaborate with clinical teams to ensure data quality and accuracy, with a focus on oncology products.Generate analysis-ready datasets for statistical analysis and reporting.Conduct statistical analyses to evaluate the safety and efficacy of oncology therapies.Prepare tables, listings, and figures (TLFs) for clinical study reports.Ensure compliance with regulatory requirements for data submissions.Contribute to the development of data quality control processes.Participate in data visualization and data cleaning tasks as needed.Stay updated with industry standards, best practices, and emerging trends in SAS programming for clinical trials.Requirements:

Bachelor's degree in a related field from a United States college or university (master's degree preferred).5+ years of experience as a SAS Statistical Programmer in the pharmaceutical, biotechnology, or clinical research industry.Deep understanding of CSDIC standards, SDTM, and ADaM.Experience working on oncology products and clinical trials.Proficiency in SAS programming, including data transformation and statistical analysis.Familiarity with regulatory submissions and compliance.Strong problem-solving and analytical skills.Excellent communication and teamwork abilities.Detail-oriented with a commitment to data quality and accuracy.

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