Associate Principal Scientist, Stat. Programming - Sdtm (hybrid)

Newyorkbioconnect

Base: $142,400.00 - $224,100.00; bonus/equity: eli...
Hybrid
Sas programming in clinical trials
Submission data standards sdtm and adam
Statistical programming leadership
The Associate Principal Statistical Programmer provides oversight and quality management of submission data standard deliverables for worldwide regulatory applications of drug and vaccine clinical development projects

Job Summary

  • The Associate Principal Statistical Programmer provides oversight and quality management of submission data standard deliverables for worldwide regulatory applications of drug and vaccine clinical development projects.
  • The position offers a comprehensive benefits package including medical, dental, vision, retirement plans, paid holidays, vacation, and sick days.
  • Employees in office-based U.S. positions will work a hybrid model with three days on-site and two days remote per week, effective September 5, 2023.

Matching Summary

The Associate Principal Statistical Programmer provides oversight and quality management of submission data standard deliverables for worldwide regulatory applications of drug and vaccine clinical development projects.

Salary

Base: $142,400.00 - $224,100.00; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Medical, dental, vision, retirement, paid holidays, vacation, sick days

Skills & Requirements

Must-have

  • SAS programming in clinical trials
  • Submission data standards SDTM and ADaM
  • Statistical programming leadership
  • Regulatory submission deliverables
  • Python and SAS technical skills
  • Project management skills
  • Hybrid work model

Nice-to-have

  • Technical writing skills
  • Process improvement experience
  • Cross-cultural collaboration
  • Mentoring and guidance
  • Experience with Microsoft Project
  • Participation in industry teams

Key Requirements

  • BA/BS plus 9 years SAS programming experience
  • MS plus 7 years SAS programming experience
  • US and/or worldwide regulatory submission leadership experience
  • Experience with CDISC standards and Define.XML
  • Ability to work in hybrid model
  • VISA sponsorship available

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter