SAS Programmer - 2-10 Years
Experience required of statistical programming in clinical/pharma domain
Strong programming and analytical skills using SAS software
Proven experience in producing Statistical Outputs (TLGs in Safety/Efficacy) from the provided specifications/documents
Responsible for the accuracy of SAS programs by reviewing output, reviewing code, reviewing log files and running all checking utilities.
Good knowledge and understanding of CDISC SDTM , ADaM and Define.xml standards
Strong knowledge of regulatory guidance documents such as ICH-E3 and ICH-E9
Graduate in Mathematics/ Statistics/ Applied statistics / Computer Science / Life Sciences
Bio-Stats Reporting - 2-10Years
Development of Statistical Analysis Plan (SAP) or equivalent including Table Shells Design.
Provide statistical support for case report form design, database development, data validation plan and blinded data review as and when required.
Conduct literature searches to support statistical analysis.
With minimal or no oversight, perform statistical programming in SAS to generate tables, listings, figures, and statistical analysis for efficacy outputs.
Author the statistical report and provide statistical inputs to clinical study report
Ability to perform Adhoc analysis
Comply with project / trial standards and specifications following internal guidelines as well as the guidelines set by the various health authorities.
Participate in client or regulatory audits.
Guide cross functional teams Data management and medical writers for all trial related activities
M.Sc. or a higher degree (Statistics/ Biostatistics/ Mathematical Statistics/ Applied Statistics)
Experience required of statistical programming in clinical/pharma domain
Strong programming and analytical skills using SAS software
Proven experience in producing Statistical Outputs (TLGs in Safety/Efficacy) from the provided specifications/documents
Responsible for the accuracy of SAS programs by reviewing output, reviewing code, reviewing log files and running all checking utilities.
Good knowledge and understanding of CDISC SDTM , ADaM and Define.xml standards
Strong knowledge of regulatory guidance documents such as ICH-E3 and ICH-E9
Graduate in Mathematics/ Statistics/ Applied statistics / Computer Science / Life Sciences
Bio-Stats Reporting - 2-10Years
Development of Statistical Analysis Plan (SAP) or equivalent including Table Shells Design.
Provide statistical support for case report form design, database development, data validation plan and blinded data review as and when required.
Conduct literature searches to support statistical analysis.
With minimal or no oversight, perform statistical programming in SAS to generate tables, listings, figures, and statistical analysis for efficacy outputs.
Author the statistical report and provide statistical inputs to clinical study report
Ability to perform Adhoc analysis
Comply with project / trial standards and specifications following internal guidelines as well as the guidelines set by the various health authorities.
Participate in client or regulatory audits.
Guide cross functional teams Data management and medical writers for all trial related activities
M.Sc. or a higher degree (Statistics/ Biostatistics/ Mathematical Statistics/ Applied Statistics)
Address :
+Cognizant Technology Solution
2nd Floor , Mindspace building no 9 ,
Opp Airoli Railway Station , Airoli
Timings : 9.30am - 10.00am
Please carry your photo or photo id proof.