Clinical SAS Programmer
Katalyst Healthcares and Life Sciences
Responsibilities & Requirements:
- Provide statistical programming support for clinical trial data reporting under the general guidance of a biostatistician.
- Develop SAS programs that generate tables, listings and figures and derived datasets that summarize results for clinical trials.
- Contribute to the development and implementation of programming and reporting standards.
- Contribute to the development of a macro library.
- Work closely with data management to assure data quality and consistency.
- Provide occasional analytical support under the supervision of a biostatistician.
- These efforts must meet company objectives and satisfy regulatory GCP and ICH requirements and guidelines.
- Must have experience with SDTM & ADaM.
- Must have at least 7 years of pharma industry.
Vacancy posted 7 hours ago
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