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Lead SAS Programmer

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Brief description :

  • Process oriented qualified statisticians having 4-8 years of strong experience in SAS programming and project management in clinical research domain
  • Experience in leading and building high performing teams
  • Deep understanding of the complete clinical trial process
  • Good understanding of the regulatory requirements namely ICH/GCP guidelines
  • Experience in generation , maintenance and implementation of SOPs/guidelines
  • Experience in SAP/Shell development and report writing
  • Extensive experience in the areas of TFL generation and CDISC Migration
  • Capable of handling quality audits
  • Guide the team in continued professional and technical growth
  • Will be required to attend conferences and present papers and support in business development
  • Support the HR department with inputs on resource requirement, hiring and performance matrix/evaluation.

Preferred skills


  • Project Management
  • Statistics
  • SAS Programming
  • CDISC Migration