Hi Friends, Duration: 24 months (perhaps longer depending on the study.)
Location: Chicago. *ESSENTIAL FUNCTIONS:* 1. To provide SAS programming support for the Clinical Research Programming Department. 2. Develop and document programs to create analysis datasets summarizing key clinical trial data. 3. Develop and document programs and to produce tables, listings and other reports and analyses summarizing clinical trial results. 4. Perform and document quality control checks for programs. 5. Assist in testing and implementation of new and updated internally and externally developed software as well as new SAS releases. *OTHER RESPONSIBILITIES / DETAILED DUTIES:* 1. Participate in the development and review of study-specific procedures; participate in clinical project team meetings as required. 2. Assist with the development of case report forms. This is not an exhaustive, comprehensive listing of job functions. May perform other duties as assigned. *Related Experience:* 1. Minimum of 5 years experience programming and analyzing scientific data in a pharmaceutical / clinical trial environment. 2. Expertise in SAS programming language. *Resumes with the following information will be given preference.* *Full Name:* *Current Location:* *Relocation:* *Availability:* *Work Authorization in US:* *Contact Number:* *Email:* *Rate on C2C:* *Please ensure all candidates have all skills listed under "Required Skills" in their resume.* *Reply - pa...@everestcom.com* -- You received this message because you are subscribed to the Google Groups "Oracle-Projects" group. To post to this group, send email to oracle-projects@googlegroups.com. To unsubscribe from this group, send email to oracle-projects+unsubscr...@googlegroups.com. For more options, visit this group at http://groups.google.com/group/oracle-projects?hl=en.
