Advanced Statistical Programming Leader for Clinical Trials

3 days ago


Canada Warman O'Brien Full time
Statistical Programmer Role Overview

We're partnering with a small CRO experiencing significant growth in Biometrics.

The Job:
  • Lead high-impact projects, tackling complex statistical programming tasks and managing project timelines.
  • Work directly with clients and regulatory agencies, ensuring data quality and delivering programming solutions for clinical trials.
  • Mentor junior team members, contribute to regulatory submissions, and develop new programming tools.
Key ResponsibilitiesTechnical Expertise
  • Lead statistical programming for complex projects, solving intricate challenges while ensuring project delivery meets quality standards.
  • Create and validate SDTM and ADaM dataset specifications, ensuring adherence to SOPs.
  • Program and validate datasets, ensuring accuracy and data integrity.
Collaboration and Leadership
  • Collaborate with clients, providing programming oversight, project estimates, and participating in bid defenses.
  • Mentor junior programmers and lead project teams, fostering development and collaboration.
Requirements
  • Master's or Ph.D. in Statistics, Biostatistics, Epidemiology, or Computer Science.
  • 6+ years of clinical trial statistical programming experience with an advanced degree, or 8+ years with a Bachelor's degree.
  • Experience working with clinical trial data, SDTM/ADaM datasets, and regulatory submissions.
Compensation

$120,000 - $150,000 per year, based on experience and qualifications.

What We Offer

Opportunities for professional growth and development, collaborative work environment, and competitive compensation package.



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