Stastical Programmer

My client is an innovating, dynamic and growing international pharmaceutical company, looking for a **Statistical Programmer **with a strong experience with SAS programming and CDISC.

As the new Statistical Programmer, you will be responsible for leading, developing and implementing statistical solutions to the company R&D sponsored clinical trials. Within this role, you will perform statistical programming activities for all assigned clinical studies sponsored by the company.

**Responsibilities**:

- Provide statistical programming expertise with respect to Statistical Programming, Biostatistics
- Perform/Coordinate all statistical programming related tasks
- Support the development of tables, listings and figures for assigned projects
- Work closely with statisticians to deliver all the statistical deliverables
- Create derived data set specifications for all assigned studies and integrated summaries
- Provide oversight and guidance to CRO for all statistical programming related activities, including development and validation of ADaM
- Review statistical analysis plans for all assigned studies and integrated summaries and provide comments to study biostatistician
- Review annotated case report forms and provide comments
- Contribute to process improvement initiatives as assigned

**Minimum Requirements**:

- Minimum of 6-7 years of SAS Programming experience including statistical programming experience in pharmaceutical setting
- Very good knowledge of CDISC Standards, including SDTM, ADaM
- Master's or bachelor's degree in Statistics, Mathematics, Computer Science, or any related field
- Knowledge in SAS macros
- Good understanding in statistical methods used in statistical analysis
- Ability to review protocol and SAP and provide feedback
- Good understanding in Good Programming Practices in pharmaceutical industry
- Fundamental knowledge of GCP standards