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.