- Performs all SAS programming required for clinical trial analysis and reporting
- Ensures that activities and processes performed are conducted according to sponsor requirements
- Works closely with the Biostatistics and Data Management departments on various clinical projects
- Leads programming efforts for multiple studies within the company’s Consumer Healthcare
- Reviews case report form (CRF) design. Programs edit checks from the Data Management Plan specifications
- Creates derived-analysis datasets
- Executes analyses specified in the protocol or the Statistical Analysis Plan (SAP) under the guidance of the project statistician
- Acts as primary programmer to produce tables, listings, and figures for the clinical study report (CSR)
- Acts as secondary programmer to validate SAS programs that produce derived-analysis datasets and data analyses
- Postgraduate Degree Desired
- SAS Experience: Required 4-7 Years Advanced
- Statistical Analysis Required 4-7 Years
- Excellent SAS programming skills and expertise
- Strong knowledge in UNIX environment
- Good knowledge in Statistics and Data Management processes
- Good time management skills
- Advanced degree in statistics or mathematics or computer science
- Minimum of 5 years of experience in SAS programming
- Ability to communicate effectively (oral and written)
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