Job Description

Responsibilities:

Independently, perform SAS programming and analysis support of the generation of analysis datasets, statistical analysis, listings, figures and tables.

Independently, develop SAS application code.

Independently, perform validation of SAS programs and deliverables.

Independently, perform migrations and verifications.

Independently, perform SDTM and Adam mapping.

Generate SDTM and Adam deliverables.

Generate all necessary output for the compilation of statistical appendices for CTR, ISS, and Client.

Generate data files and/or output for safety updates, publications and meeting presentations.

Interface with a cross-function of client and Diabetics team members.

Requirements:

3+ years Pharmaceutical or CRO industry experience in clinical reporting and statistical programming.

Oncology clinical trial experience.

Strong competence in SAS/Base, SAS/Macro, and SAS/STAT programming.

Working knowledge of CDISC, SDTM and ADaM.

Expert knowledge of SAS-based statistical programming.

Proficiency in SAS programming on multiple platforms and operating systems, e.g. Windows, UNIX, etc. is desirable.

Job Tags

Permanent employment,

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