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
Qualifications
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.
Additional Information
Visa Status
Only US Citizens, Green Card, EAD and OPT holders.