Senior Statistical Programmer Consultant - Remote

Socket.dev

United States

Remote

USD 120,000 - 180,000

Full time

9 days ago
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Job summary

ClinChoice is seeking a Senior Statistical Programmer Consultant to join one of our client teams. This delivery-focused role operates under a programming team lead to deliver technical programming and information components of a project, with autonomy and high technical requirements.

The candidate should have 5+ years of CDISC clinical programming (6+ with a Master’s) and strong knowledge of ICH/GCP, regulatory terminology, and the clinical drug development process.

Qualifications

  • Bachelor’s degree in computer science (CS), statistics, or related discipline with 5+ years clinical programming (CDISC) experience OR Master’s with 6+ years CDISC experience.
  • Working knowledge of ICH and Good Clinical Practices, clinical research, clinical trial process, and related regulatory requirements.
  • Strong communication and coordination skills; proactive stakeholder influence in programming items.

Responsibilities

  • Deliver programming for a clinical study or project under leadership.
  • Implement statistical programming aspects of the protocol and development program.
  • Ensure high quality in your deliverables and in others’ programming work.
  • Program independently with high efficiency and quality.
  • Create and review specifications and relevant documentation.
  • Contribute to best practices to improve quality, efficiency, and effectiveness.

Skills

CDISC
Clinical programming

Education

Bachelor’s degree in CS or Statistics
Master’s degree in CS or Statistics

Job description

ClinChoice is seeking a Senior Statistical Programmer Consultant to join one of our client teams. This delivery-focused role operates under a programming team lead to deliver technical programming and information components of a project, with autonomy and high technical requirements.

The candidate should have 5+ years of CDISC clinical programming (6+ with a Master’s) and strong knowledge of ICH/GCP, regulatory terminology, and the clinical drug development process.

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