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Sr. SAS Statistical Programmer: Comsys

Job ID10-474-193
Company NameComsys
Job CategoryPharmaceutical/Biotech; Pharmaceutical/Biotech
LocationKalamazoo, MI
Position TypeFull-Time, Employee
Experience5-10 Years Experience
Date PostedNovember 15, 2009 (Reposted Dec 2)
Comsys
View Comsys profile and job listings

Sr. SAS Statisitcal Programmer



JOIN OUR TEAM

For many years, most everybody has known us as Trilogy Consulting, then Venturi Partners. Our reputation for assessing unique situations and then providing dynamic solutions has been unparalleled. In keeping with the flexibility and resourcefulness that have made us an industry standard, we're not only riding the wave of change but taking advantage of it as well.

We're now COMSYS, a nationwide provider of information technology consulting and staffing. Same great services you're used to, and quite a bit more.

Here at Comsys, you will experience cutting-edge career opportunities for professionals with creativity and a strong drive for growth and success. If you are ready for the excitement of bringing your career up to an exhilarating new level of achievement, consider Comsys.

**** ONLY INDUSTRY EXPERIENCED NEED APPLY ****

Sr. SAS STATISTICAL PROGRAMMER

Experience:
Greater than 5 years of relevant career experience programming in a clinical development environment

Education:
BA/BSc or higher degree in Computer Science, Statistics, Mathematics, Life Sciences or other related scientific subject, , or work experience equivalent

Job Description:
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. Work is to be performed in a team environment, where team members may be distributed across locations and vendors. The position is expected to share technical and work experience to improve efficiencies within the product team.

Qualifications Required:
* Excellent SAS data manipulation, analysis and reporting skills
* 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.

MUST HAVE DIRECT EXPERIENCE TO BE CONSIDERED!

Please send only appropriate resumes to:

tzeithammel@comsys.com
Reference ID #10-474-193




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