Job Description Job Summary DOCS clients include small, mid and large sized Pharmaceutical companies in addition to many leading Biotechnology, Medical Device companies and CROs. As a global partner, DOCS currently offers global resourcing solutions to our clients. Roles & Responsibilities of the position W2 or 1099 preferred 5+ years of SAS experience working for a pharma or CRO CDISC experience (both SDTM and ADaM) BS acceptable, MS preferred 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. CDISC (SDTM and ADaM) experience required - 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. Associated topics: backend, c++, c#, develop, devops, perl, php, software developer, software engineer, software programmer
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