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Accountabilities:

  • Perform end-to-end statistical programming activities for ADaM datasets, TLFs.
  • Support regulatory deliverables including ISS, ISE, submissions, and queries.
  • Develop, validate, and maintain CDISC-compliant SDTM and ADaM datasets.

Requirements:

  • 6–10+ years statistical programming in clinical research.
  • Strong hands-on R programming (1–3+ years practical).
  • Solid SAS programming with clinical trial experience.

Benefits:

  • Fully remote work opportunity.
  • Long-term contract engagement.
  • Competitive salary package.

Partner Company

The partner company is a clinical research organization that supports impactful clinical programs through statistical programming. It offers a collaborative culture and a flexible remote work environment.

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