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.