Senior Statistical Programmer — Hybrid, Global Trials
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Job summary
Merck & Co., Inc. is seeking a Senior Statistical Programmer to deliver high-quality programming for global stakeholders in Early Development Statistics and PK/PD modeling.
The role involves gathering requirements, transforming data into analysis datasets, and developing tables, listings and figures per analysis plans, partnering with statisticians and PK modelers. The ideal candidate has extensive SAS/R experience in a clinical trial environment, familiarity with CDISC SDTM/ADaM, and a strong
Qualifications
- BA/BS in related field + 5–9 years SAS/R experience in a clinical trial environment
- MS in related field + 3–7 years SAS/R experience in a clinical trial environment
- Experience with CDISC SDTM/ADaM standards
- Strong programming for data manipulation, analysis and reporting
Responsibilities
- Develop, validate and maintain complex datasets, tables, listings and figures
- Provide analytical support for exploratory analyses
- Prepare compliant code for regulatory submissions and documentation
- Ensure traceability from data source to results
- Lead programming tasks within a project and collaborate with stakeholders
Skills
Education
Tools
Job description
Merck & Co., Inc. is seeking a Senior Statistical Programmer to deliver high-quality programming for global stakeholders in Early Development Statistics and PK/PD modeling.
The role involves gathering requirements, transforming data into analysis datasets, and developing tables, listings and figures per analysis plans, partnering with statisticians and PK modelers. The ideal candidate has extensive SAS/R experience in a clinical trial environment, familiarity with CDISC SDTM/ADaM, and a strong
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