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Vacancy description

Senior Statistical Programmer 2 in Thiruvananthapuram, भारत

Worldwide Clinical Trials

Thiruvananthapuram, भारत

Senior Statistical Programmer 2 role at a global CRO involves leading programming initiatives, developing and validating clinical datasets using SAS, and providing consultancy on CDISC standards and regulatory submissions. The position requires mentoring team members and driving continuous improvement across biostatistical operations.

Responsibilities

  • Develop, test, and validate SAS programs for CDISC SDTM and ADaM datasets, tables, figures, and listings
  • Lead complex programming projects, oversee team tasks, and manage project scope and budgets
  • Review clinical database specifications and develop electronic data submission packages for regulatory compliance
  • Provide training and consultancy on CDISC standards, regulatory requirements, and programming best practices
  • Lead process improvement initiatives and develop department standard operating procedures and templates

Requirements

  • Degree-level education or equivalent qualification
  • Advanced SAS programming expertise including Macro, Proc Report, ODS
  • Minimum 6 years of related statistical programming experience
  • Expert knowledge of CDISC standards and electronic data submission requirements
  • Strong analytical skills with meticulous attention to detail
  • Ability to mentor and train programming staff and other departments

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