Sr. Statistical Programmer- i3 Statprobe- Any i3 Office

UnitedHealth Group is an innovative leader in the health and well-being industry, serving more than 55 million Americans. Through our family of companies, we contribute outstanding clinical insight with consumer-friendly services and advanced technology to help people achieve optimal health.

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 currently have a need for an experienced Sr. Statistical Programmer for any one of our i3 offices; Ann Arbor, MI, Austin, TX, Basking Ridge, NJ, Cary, NC, Lexington, KY, San Diego, CA, or Westerville, OH



The Senior Statistical Programmer is a member of the Biostatistics team and plays a lead role in performing all SAS programming required for clinical trial analysis and reporting. The Senior 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.

Job Requirements:
B.S. degree required, M.S. degree preferred.
A minimum of five 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.

Diversity creates a healthier atmosphere: an equal opportunity employer, M/F/D/V.