Statistical Programmer Consultant

New

Skills

Clinical Research Documentation Documentation Management Medical Quality Assurance Sas Programming Statistical Analysis Statistics Team Coordination

Join ClinChoice as a Senior/Principal Statistical Programmer Consultant, where you'll work directly with a single sponsor while enjoying the career growth and stability provided by a global CRO. This remote client-facing role requires independence, technical excellence, and the ability to build high-trust relationships. You will support programming efforts for clinical studies, ensuring high-quality deliverables, compliance with standards, and collaboration across multidisciplinary teams.

Key Responsibilities
  • Support and deliver programming for clinical studies and projects.
  • Implement statistical programming aspects of clinical protocols and development programs.
  • Ensure high quality in deliverables and oversee quality from other programmers.
  • Write and implement programming specifications and maintain documentation.
  • Contribute to best practices for quality, efficiency, and effectiveness within the function.
  • Ensure compliance with industry standards and promote automation usage.
  • Plan and support team activities, escalating risks as needed.
  • Collaborate proactively with statisticians, lead programmers, data managers, and study leaders.
Required Skills & Qualifications
  • Bachelor's or Master's degree in Computer Science, Statistics, or related discipline.
  • Minimum 5 years (Bachelor's) or 6 years (Master's) of clinical programming experience (CDISC required).
  • Oncology Therapeutic Area experience.
  • Strong knowledge of ICH-GCP, clinical research, trial processes, and regulatory requirements.
  • Excellent communication and coordination skills.
  • Proficiency in managing concurrent project activities and influencing stakeholders.
  • Up-to-date knowledge of technical and regulatory requirements.

Job Type: Remote

Salary: Not Disclosed

Experience: Entry

Duration: 12 Months

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