Job Title : Senior Statistical Programmer
Description
This is a challenging role that involves working with clinical trial data in the Pharmaceutical and Biotech industry. As a Senior Statistical Programmer, you will be responsible for leveraging your advanced SAS programming skills to support or lead one or more Phase I-IV clinical trials.
Responsibilities :
- Data manipulation, analysis, and reporting of clinical trial data, both safety and efficacy (ISS / ISE), utilizing SAS programming
- Generating and validating SDTM and ADaM datasets / analysis files, and tables, listings, and figures (TLFs)
- Production and QC / validation programming
- Generating complex ad-hoc reports utilizing raw data
- Applying strong understanding / experience of Efficacy analysis
Requirements
To be successful in this position, you will have :
Bachelor's degree in Statistics, Computer Science, Mathematics, etc.At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor's degree or equivalent.Strong SAS data manipulation, analysis, and reporting skills.Solid experience implementing the latest CDISC SDTM / ADaM standards.Good ad-hoc reporting skills.Proficiency in Efficacy analysis.About Us
We are a dynamic team committed to delivering high-quality results in a globally dispersed team environment. We value collaboration, intellectual curiosity, and innovation.