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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 ****
TECHNICAL SAS PROGRAMMING MANAGER
Greater than 7 years of relevant career experience programming in a clinical development environment. Includes at least 3 years experience as line manager, lead programmer (managing resources and time lines), or project manager
Education:
BA/BSc or higher degree in Computer Science, Statistics, Mathematics, Life Sciences or other related scientific subject, , or work experience equivalent
Job Description:
The position is a lead role designated to manage a team of programmer/analysts that includes ensuring time lines and quality standards are met. Also manages tasks assigned to his/her staff to ensure assignments match programmers abilities, and provides training to junior programmers. The Technical Programmer Manager will ensure time lines and quality standards are met, and will manage tasks assigned to his/her staff to ensure assignments match programmers abilities. Hands-on statistical programming is also an expectation for the role. 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.
Qualifications Required:
* Ability to lead and manage programmer/analysts in the successful and timely completion of clinical trial data manipulation, analysis and reporting
* 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
