• Minimum 2-3 years of experience defining SAS analysis requirements and performing SAS programming
• BASE SAS cert
• Expert knowledge of base SAS and SAS Macros for SAS software development
• Design, development and unit-testing od SAS program code, functions and scripts to efficiently extract, merge and manipulate data
• Expert Knowledge of lookup tables for SAS for SAS software development
• Expert knowledge in proposing and implementing improvements/efficiencies for SAS software development to create repeatable business processes for use by others
• Excellent oral and written communication skills in English
• Experience clarifying business and technical requirements with data requestors
• Provides technical and analytic input to peer review team

Education:

• BA/BS or equivalent experience in mathematics, statistics computer science, life sciences or related field.

 Additional skill set:

• Expert knowledge of/experience with SAS software. 
• Good understanding of global clinical trials practices, procedures, methodologies.
• Good understanding of regulatory requirements relevant to SR (e.g. GCP, ICH) 
• Experience in providing recommendations for maintenance or development of SR global policies, procedures and clinical data presentation standards. 
• Intermediate knowledge of office tools. 
• Experience in a pharmacetical company is must.

Visa Status

• Only US Citizens, Green Card, EAD and OPT holders.
• No H1B Holders and Third-Parties.
• No Corp-Corp