Job Description

Job Responsibilities:

• Provides input for Budget Planning
• Likely to oversee contingent workers and/or vendors; Likely to provide training to others
• Primarily works at the project level
• Delivers assignments with quality and within timelines
• Contributes strategy under moderate supervision
• Provides strong programming support to CDISC based e-submission. Develop, review, and/or perform validation of generic macros. Develop, debug, and enhance SAS programs to support quality control of safety or efficacy derived datasets
• Has good knowledge and understanding of statistical models in efficacy data analysis
• Responsible for the standardization of Clinical Programming deliverables within a project
• Extends existing or develops new clinical programming methods to solve complex problems

Skills:

• Experience in SDTM and ADaM acquainted with CDISC Guidelines and requirements.
• Specialized or Technical Knowledge Licenses, Certifications needed:
• Functional Knowledge:
• Advanced level of SAS programming skills. Develop SAS programs and perform QC tasks for integrated analysis.

Education/Experience:

• Education Required: Bachelor’s Degree/ Master’s Degree/ PhD in Science, Statistics, Information Technology or equivalent combination of education and related work experience.
• Experience Required: Bachelor’s + 5 years or Master’s + 4 years of professional experience in a pharmaceutical or clinical research setting as a programmer

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