Clinical SAS Programmer

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.