Principal SAS Programmer Loc:Overland Park, Kansas
Cambridge, MA
100,000 - 200,000
Job Description:
Role:Principal SAS Programmer
Location :Overland Park, Kansas
Implementing your know-how and experience with CDISC standards, in both SDTM and AdaM;performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy;creating analysis files, tables, listings, and figures (TLFs), validating those files, maintaining associated tracking and validation documentation;creating and validating CDISC, SDTMs and ADaM.
What we need from you:
- Bachelor's degree or equivalent, preferably in a scientific discipline such as Statistics, Mathematics, Computer Science, etc.
- 8+ years of SAS programming supporting clinical trials for the Pharmaceutical / Biotech industry, with experience working for a CRO (required).
- 3+ years study lead experience juggling mutliple studies/projects simultaneously.
- Familiarity with drug development life cycle and strong proficiency with the manipulation, analysis and reporting of clinical trials data.Strong SAS data manipulation, analysis and reporting skills.
- Ability to implement the latest CDISC SDTM / ADaM standards, and define.XML.
- Ability to provide quality output and deliverable, in adherence with challenging timelines.Strong QC / Validation experience.
- Self-motivated, with excellent time-management and multi-tasking skills.
- Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.
- Ability to handle ad-hoc requests with minimal guidance.Submissions experience required.Excellent organizational, oral and written communication skills.Knowledge of R programming is a plus.