SAS programmer - Katalyst Healthcares & Life Sciences
South Plainfield, NJ 07080
About the Job
Responsibilities:
- The senior statistical programmer will be responsible for supporting regulatory RWE studies and ensuring that the study programming teams understand and comply with the appropriate regulatory processes and data standards.
- Additionally, the senior statistical programmer will develop templates, macros, and other resources to increase programming efficiencies and mitigate risks.
- Candidates must have excellent SAS and SQL programming skills and the ability to implement complex logic.
- Prior experience designing and creating SDTM and/or ADaM datasets from real-world data (RWD) is strongly desired.
- Strong communication, time management, enthusiasm, and documentation skills are essential in this home-based position.
- I'm looking for an experienced SAS programmer with 4 years industry experience working with RWD (Real world data) claims.
- Master's degree in Epidemiology, Biostatistics, Computer Science, or other subjects with high statistical content.
- Minimum four years SAS statistical programming experience.
- Database programming using SQL.
- Experience with real world healthcare data such as MarketScan, Optum, EMR, PharMetrics, and/or Medicare databases.
- Experience designing and generating datasets in SDTM and/or ADaM.
- Training or experience with R, Databricks, Spark SQL, or Python.
- Training or experience in the pharmaceutical industry.
- Training or experience in epidemiological methods.
- Experience with validating data and generating reports in Pinnacle 21 (P21).
- EHR and EMR data such as MarketScan, Optum and Medicare databases. Experience with advanced statistical methods such as survival and regression and hands on CDISC/SDTM/ADaM experience.
Source : Katalyst Healthcares & Life Sciences