Posted to MedZilla on 2/9/2018

DOCS Global, Inc.

US-CA, Clinical SAS Programmer EZ-4603-MZ


Sr.Programmer for study support: TFLs, validation, documentation, communication, SDTM/ADaM, teamwork - hit the ground running in SAS, UNIX, and clinical trials reporting.

Sr. Programmer Basic Qualifications:
" BA/BSc or higher degree in Computer Science, Statistics, Mathematics, Life Sciences or other related scientific subject, or work experience equivalent
" Greater than 5 years of relevant career experience programming in a clinical development environment
" Excellent SAS data manipulation, analysis and reporting skills
" Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data
" Ability to work effectively and successfully in a team environment
" Excellent oral and written communication skills
" Ability to provide quality output and deliverables, in adherence with challenging timelines
" Willingness and ability to learn and follow standard processes and procedures.
Key Responsibilities:
Programming includes, but is not limited to, the data manipulation, analysis and reporting of primarily clinical trial data. Specifically, analysis files creation; table/listing/graph generation; program validation and documentation; and output verification. Work is to be performed in a team environment, where team members may be distributed across locations and Suppliers.

NOTE: This is a work from home opportunity for a seasoned SAS Programmer.

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