- Statistical Programmers : 3 - 5 Yrs.
- Senior or a Lead SAS Programmer - 5 - 9 Yrs.
- Principal or Sr.Principal Programmers - 9+ yrs.
Job Description:
- Locally coordinate and take responsibility for trial level programming activities (analysis datasets, pooled datasets, listings, tables and figures) of individual Phase I-IV clinical trials to support program programmers and statistician in project level activities.
- Be responsible for statistical tasks on assigned clinical trials e.g. RAP.
- Maintain efficient interfaces with internal and external customers with support of ONC Biometrics management and the Program Programmer/Statistician.
- Make certain that documents and specifications are consistent and comply with company standards by providing input into CRF and data structures tables, listings and figures for phase I-IV clinical trials and submission activities.
- Program and deliver, according to specifications, analysis datasets, pooled datasets, listings, tables, and figures for phase I-IV clinical trials and for pooled analysis with high quality and within milestones.
- In consultation with the statistician, develop specifications for analysis datasets, pooled datasets, and listings
- Maintain records for all assigned projects and archiving of trial / project analysis and associated documentation.
- Provide input on process improvement initiatives and participate in non-clinical project activities with support from GH
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- Senior or a Lead SAS Programmer - 5 - 9 Yrs.
- Principal or Sr.Principal Programmers - 9+ yrs.
Job Description:
- Locally coordinate and take responsibility for trial level programming activities (analysis datasets, pooled datasets, listings, tables and figures) of individual Phase I-IV clinical trials to support program programmers and statistician in project level activities.
- Be responsible for statistical tasks on assigned clinical trials e.g. RAP.
- Maintain efficient interfaces with internal and external customers with support of ONC Biometrics management and the Program Programmer/Statistician.
- Make certain that documents and specifications are consistent and comply with company standards by providing input into CRF and data structures tables, listings and figures for phase I-IV clinical trials and submission activities.
- Program and deliver, according to specifications, analysis datasets, pooled datasets, listings, tables, and figures for phase I-IV clinical trials and for pooled analysis with high quality and within milestones.
- In consultation with the statistician, develop specifications for analysis datasets, pooled datasets, and listings
- Maintain records for all assigned projects and archiving of trial / project analysis and associated documentation.
- Provide input on process improvement initiatives and participate in non-clinical project activities with support from GH
Please share this to your network, to help someone waiting for an opportunity to work with Novartis Health care.
You are requested to carry the following documents:
- 2 copies of Resume
- Recent 3 Months Salary slips
- Detailed salary breakup (Offer letter / Appraisal letter)
Job location : Hyderabad.
Note :Only the applicants/ direct walk-ins with 3yrs and above of relevant experience in Clinical SAS would be considered for the interview
Note :Only the applicants/ direct walk-ins with 3yrs and above of relevant experience in Clinical SAS would be considered for the interview
Walk-in -Date : 18 FEB 2017 @ 9:00 AM (Saturday)
Venue:
Novotel Bengaluru Techpark,
Opposite RMZ Ecospace Business Park,
Marathahalli - Sarjapur Outer Ring Road,
Bengaluru 560103, Karnataka, India
T: +91 (80) 66700600 I M: +91 9538897361 .
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