Urgent need of SAS Programmer @ Round Lake, IL
*Please send resumes to aja...@shstinc.com aja...@shstinc.com or call me 412 450 1316 X 202* *Gtalk: aijaz.recruiter* *Job Title: SAS Programmer* *Location: Round Lake, IL* *Duration: 6+ months* *Job Description:* SAS Programmer Pharma Healthcare Experienced SAS Programmer for all phases of clinical trials. *Duties:* (1) Develop Programs that convert raw SAS datasets to standard format. (2) Develop Programs that produce analysis datasets from raw data or standard data. (3) Program Data Displays (Tables, Listings, Graphs) for inclusion in documents including publications, stat reports, clinical study report and other regulatory documents. (4) Peer review of SAS Programming Code and deliverables (derived data, tables, listings graphs). (5) Participate in project meetings. (6) Prepare documentation on above production programming and validation activities. *Experience:* Strong programming skills in technologies used and experience in all phases of clinical trials. Possess data analysis and problem solving skills; familiarly with clinical trial database; strong written and verbal communication skills. *Requirements:* Bachelor’s degree plus 3+ years of SAS experience in the medical devices or pharmaceutical industry. -- You received this message because you are subscribed to the Google Groups CorptoCorp group. To unsubscribe from this group and stop receiving emails from it, send an email to corptocorp+unsubscr...@googlegroups.com. To post to this group, send email to corptocorp@googlegroups.com. Visit this group at http://groups.google.com/group/corptocorp. For more options, visit https://groups.google.com/d/optout.
Urgent need of SAS Programmer @ Round Lake, IL
*Please send resumes to aja...@shstinc.com aja...@shstinc.com or call me 412 450 1316 X 202* *Gtalk: aijaz.recruiter* *Job Title: SAS Programmer* *Location: Round Lake, IL* *Duration: 6+ months* *Job Description:* SAS Programmer Pharma Healthcare Experienced SAS Programmer for all phases of clinical trials. *Duties:* (1) Develop Programs that convert raw SAS datasets to standard format. (2) Develop Programs that produce analysis datasets from raw data or standard data. (3) Program Data Displays (Tables, Listings, Graphs) for inclusion in documents including publications, stat reports, clinical study report and other regulatory documents. (4) Peer review of SAS Programming Code and deliverables (derived data, tables, listings graphs). (5) Participate in project meetings. (6) Prepare documentation on above production programming and validation activities. *Experience:* Strong programming skills in technologies used and experience in all phases of clinical trials. Possess data analysis and problem solving skills; familiarly with clinical trial database; strong written and verbal communication skills. *Requirements:* Bachelor’s degree plus 3+ years of SAS experience in the medical devices or pharmaceutical industry. -- You received this message because you are subscribed to the Google Groups CorptoCorp group. To unsubscribe from this group and stop receiving emails from it, send an email to corptocorp+unsubscr...@googlegroups.com. To post to this group, send email to corptocorp@googlegroups.com. Visit this group at http://groups.google.com/group/corptocorp. For more options, visit https://groups.google.com/d/optout.
