Director Stat. Programming - Sdsqm (hybrid)

microsatsystems.biz

Base: $190,800.00 - $300,300.00; bonus/equity: ann...
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Cdisc data standards expertise
Regulatory submission deliverables
Clinical trial programming
** The position of Director of Statistical Programming at microsatsystems.biz involves leading a team responsible for ensuring compliance with regulatory data standards in the pharmaceutical industry. The role requires extensive experience in statistical programming within clinical trials and offers a hybrid work model with competitive compensation and benefits. **

Job Summary

  • Lead a team of submission consultants and provide advisement to ensure study data deliverables are compliant with regulatory agency requirements.
  • Apply domain and management expertise to set and achieve operational and strategic objectives, managing broad initiatives and contributing to departmental objectives.
  • The successful candidate will be eligible for annual bonus and long-term incentive, if applicable, and a comprehensive package of benefits including medical, dental, vision, and retirement benefits.

Matching Summary

Match Score: 75

** The position of Director of Statistical Programming at microsatsystems.biz involves leading a team responsible for ensuring compliance with regulatory data standards in the pharmaceutical industry. The role requires extensive experience in statistical programming within clinical trials and offers a hybrid work model with competitive compensation and benefits. **

Salary

Base: $190,800.00 - $300,300.00; Bonus/Equity: Annual bonus and long-term incentive, if applicable; Benefits: Comprehensive package of benefits

Skills & Requirements

Must-have

  • CDISC data standards expertise
  • Regulatory submission deliverables
  • Clinical trial programming
  • Statistical analysis and reporting
  • People management responsibilities

Nice-to-have

  • Strategic thinking and implementation
  • Process improvement initiatives
  • Cross-cultural collaboration
  • Active in professional societies

Key Requirements

  • BS plus 12 years or MS plus 10 years experience
  • 2 years statistical programming in clinical trials
  • 7+ years project management experience
  • US and/or worldwide drug/vaccine regulatory submission experience
  • Experience leading programming teams with global resources

Work Rights

Not specified

Tailored Resume

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