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Clinical SAS Programmer

Remote:

Full Remote

Experience:

Senior (5-10 years)

Work from:

Connecticut (USA), Illinois (USA)

Offer summary

Strong SAS programming skills in Windows UNIX environment, Experience with clinical trial standards (CDISC, SDTM, ADaM).

Katalyst HealthCares & Life Sciences Pharmaceuticals SME https://www.katalysthls.com/

51 - 200 Employees

Responsibilities:

Independently develop/validate programs that generate SDTM and analysis datasets based on ADaM specifications.
Prepare/QC ADaM datasets documentation: Define.xml, Reviewer's Guide and analysis metadata report.
Independently develop/validate programs that generate tables and listings specified in the protocol or the Statistical Analysis Plan (SAP).
Perform quality control on final reports
Provide QC and validation reports.
Support development of technical programming specifications for ADaM standards.
Communicate with programming and statistics leads, data managers and other team members.
Provide project progress updates of programming activities.

Requirements:

Strong SAS programming skills required in Windows & UNIX environment with proficiency in SAS/Base, SAS Macros, SAS/Stat.
Knowledge of working in SAS Grid environment with experience in SAS Enterprise Guide and SAS Studio is a plus.
Experience with all clinical phases I, II, III and IV of trails is desirable
Good understanding of standards specific to clinical trials such as CDISC, SDTM, ADaM, MedDRA, WHODRUG.
Strong problem-solving skills.
BS/MS in Statistics, Biostatistics, Computer Science, Mathematics or Life Sciences.
7+ years of statistical programming experience in the Pharmaceutical, Biotechnology, or Contract Research Industry.