SAS programmer

Company:  Katalyst Healthcares & Life Sciences
Location: South Plainfield
Closing Date: 16/10/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
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.

Requirements:

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.

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