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Principal Statistical Programmer - Late Phase Clinical - Remote

Posted 2 weeks ago

Overview

As a Principal Statistical Programmer, you will lead programming activities in late-phase clinical trials focusing on Cardiovascular, Renal, and Metabolism (CVRM), ensuring high-quality deliverables and compliance with industry standards.

In Short

  • Lead programming delivery for CVRM projects.
  • Implement statistical programming for clinical protocols.
  • Ensure high quality of project deliverables.
  • Drive best practices in programming.
  • Manage risks in complex projects.
  • Provide expert guidance to project teams.
  • Ensure compliance with regulatory requirements.
  • Mentor junior programming staff.
  • Contribute to process improvement initiatives.
  • Maintain expertise in industry standards.

Requirements

  • Bachelor’s degree in Computer Science, Statistics, or related field.
  • 8+ years of SAS programming experience.
  • Experience with CDISC standards.
  • Knowledge of ICH and GCP.
  • Strong understanding of clinical drug development.
  • Excellent communication skills.
  • Proficient in risk management.
  • Ability to influence stakeholders.
  • Experience in leading cross-functional teams.

Benefits

  • Work for a global CRO with a supportive culture.
  • Opportunities for professional development.
  • Engage in meaningful work in drug development.
  • Collaborate with diverse teams globally.
  • Contribute to a healthier and safer world.

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