Statistical Programmer | Remote
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We are looking for a skilled Statistical Programmer to support clinical research studies through statistical programming, clinical data validation, and the development of high-quality statistical deliverables.
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β’ Develop, maintain, and validate SDTM and ADaM datasets for clinical trials.
β’ Program Tables, Listings, and Figures (TLFs) for interim analyses, data monitoring, and clinical study reports.
β’ Develop and validate annotated Case Report Forms (aCRFs).
β’ Perform data cleaning activities and resolve statistical data issues in collaboration with Data Management and Biostatistics teams.
β’ Develop and maintain dataset specifications, Define-XML, and Reviewerβs Guides.
β’ Validate SDTM and ADaM datasets using Pinnacle 21.
β’ Utilize SAS macros and programming standards to improve efficiency and quality.
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β’ Bachelor's degree in Statistics, Computer Science, or a related field.
β’ At least 1 year of clinical research experience, including 1 year of Statistical Programming experience in the biotechnology, pharmaceutical, or CRO industry.
β’ Strong working knowledge of SAS.
β’ Good knowledge of CDISC standards (SDTM and ADaM).
β’ Exposure to clinical trial data, Statistical Analysis Plans (SAP), TLF Shells, and programming specifications.
β’ Knowledge of Pinnacle 21 and XML programming is an advantage.
β’ Familiarity with ICH guidelines, GCP, and FDA/Health Canada regulatory requirements.
β’ Excellent analytical, organizational, and problem-solving skills.
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