Job Description

Target Pay Rate: 60-80/hr **salary will be commensurate with experience 

• Performing programmatic review and validation of analysis datasets and TLFs, review ADaM specifications and datasets as per CDISC ADaMIG, review submission data package as per submission requirement.
• Effectively review and comment on vendor programming deliverables and help resolve technical difficulties.
• Supporting ad-hoc analysis and regulatory response, work with Biostatistics and Data Management members to support studies.
• Develop SAS coding for generating ADaM datasets and TLFs to support clinical study analysis, perform clinical study report and/or exploratory analysis for studies.
• Perform validation of ADaM datasets and TLFs per SAP.
• This position is for a Phase IV study and candidate will be involved doing adhoc request.

• Minimum of 5 years of relevant of SAS experience in major pharma or CRO
• Proficient computer skills across multiple applications and OS environments.
• Expertise with reporting tools; SAS, J-Review, and Spotfire are preferred.
• Knowledge of industry standards; CDISC-SDTM/CDASH preferred.
• Experience with external data handling of study data preferred.

• BS or above in computer science/statistics.

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