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January 16, 2008
Principal Statistical Programmer
i3 Statprobe provides a full range of data management and biostatistical services for the pharmaceutical and biotechnology industries. We not only pay relentless attention to the details, we also lend a broader perspective to a client's data management needs. We realize that strategy is just as important as process, and we provide a higher level of thinking for data management and biostatistics. As a UnitedHealth Group company, i3 Statprobe is part of a worldwide health care service organization that uses innovation, integrity and commitment to prepare for the future - and you can prepare for yours with us. It's a rare combination for success that only a career with i3 Statprobe can provide.
We are looking for talented senior-level clinical statistical programmers to join our team at one of our following facilities: Ann Arbor, MI, Austin, TX, Cary, NC, Eden Prairie, MN, Lenexa, KS, Lexington, KY, San Diego, CA, or West Chester, OH.
Principal Statistical Programmer
The Principal Statistical Programmer must ensure that activities and processes performed are conducted according to UHG and sponsor requirements. This position works closely with the Biostatistics and Data Management departments on various clinical projects.
• Leads programming efforts for large complex studies.
• This position requires time and resource management skills, and strong SAS programming expertise, and experience with pharmaceutical studies. Act as a representative of the Biostatistics department on project teams. Attend project team meetings as necessary.
• Perform all SAS programming required for clinical trial analysis and reporting.
• Provide statistical programming expertise for project teams.
• Generate tables, listings, and graphs as required.
• Assist with statistical quality assurance review and program validation for each project.
• Interact with other departments, such as Clinical Operations and Project Management, to ensure a high level of client satisfaction through successful execution of projects.
Education:
• B.S. degree required, M.S. degree preferred.
Experience:
• A minimum of ten years of experience in SAS programming for pharmaceutical projects.
• Ability to work in a fast-paced, team-oriented environment.
• Computer proficiency is mandatory.
• Ability to read, analyze, and interpret common scientific and technical journals.
• Demonstrated ability to perform statistical programming for all types of clinical trials.
• Excellent interpersonal and communication skills (written and verbal).
• Possess a positive attitude and works well with others.
For more information on i3, please visit our website: www.i3global.com
You may apply directly through UnitedHealth Group's website: http://www.unitedhealthgroup.com/careers/
Or contact:
Aaron S. Litwin
Sr. Recruiter • i3
Aaron.litwin@i3statprobe.com
i3 is proud to be an EOE/AA employer.
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