• $104,115.00 -159,340.00/year*
  • Malden , MA
  • Scientific Research
  • Full-Time
  • 29 Bryant St

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

* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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