SIRO Clinpharm is a leading full service Clinical Research Organization that specializes in providing solutions to the twin challenges of speed and cost in clinical drug development. We have pioneered the development of alternative geographies for conducting clinical trials, providing world class facilities, expertise and unexplored patient pools.
Post: Data Management/ Statistics { SAS Programmer }
Job Description:
· Creating and validating SAS programs of tables, figures and listings (TFL) for standard safety outputs in required format. Standard safety outputs could include:
o AE
o Con Med
o Labs
o Med Hist
o Vital Signs
o Physical Examination
·Creating and validating SAS programs of TFLs for efficacy outputs as per specifications provided by the lead study statistician
·Performing any other assigned activities towards programming in SAS for analyzing data
Functioning QR (Quality Review) SAS programmer for a study as applicable.
Additional Information:
Experience: 2-4 years
Location: Mumbai
Education: B.Pharm, B.Sc
Industry Type: Pharma/Biotech/Clinical Research
Functional Area: SAS Programmer
Apply/Send resume at, hr@siroclinpharm.com
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