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Clinical SAS Programmer

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Clinical SAS Programmer in remote new

  • Tata Consultancy Services
  • Full time
  • Email

Roles and Resposibilites : Be familiar with and follow the departmental and company standard operating procedures (SOPs) and working practices (WPs). Serve as a lead statistician on selected single projects. Ensure projects are well documented consistent with company SOPs and working practices. Time management of own and team's time spent on projects. Interact with the sponsor on statistical aspects of the project. Produce sample size calculations. Provide input into study design and statistical considerations, during protocol development. Review protocols for completeness, appropriateness of clinical design and sound statistical analysis. Contribute to writing appropriate protocol sections. Provide randomization schemes and appropriate documentation, on selected projects. Develop statistical analysis plans, including table, listing and graph specifications. Specify the general structure of the analysis database, provide programming support for its development and validation. Produce statistical analyses and statistical appendices, with appropriate documentation. Validate statistical analyses and statistical appendices, with appropriate documentation. Prepare Statistical Reports, Integrated Summaries of Safety, Integrated Summaries of Efficacy and other documents, as required. Contribute statistical methods section for Integrated Clinical Statistical Reports. Review Integrated Clinical Statistical Reports. Freshers can Apply

3.5 - 3.8 LPA



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