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

Imsapharma Com Ar

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 follow a hybrid work model with three days on-site and two days remote per week.

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
  • Project management skills
  • Python programming
  • Quality assurance of deliverables

Nice-to-have

  • Technical writing skills
  • Process improvement experience
  • Mentoring and guidance abilities
  • Cross-cultural collaboration
  • Experience with Microsoft Project
  • Participation in industry conferences
  • Knowledge of clinical data management

Key Requirements

  • BA/BS plus 9 years SAS programming experience
  • MS plus 7 years SAS programming experience
  • Experience in US and/or worldwide regulatory submissions
  • Knowledge of CDISC standards and Define.XML
  • Strong project management and leadership experience
  • Ability to work with global outsource partners
  • Visa sponsorship available

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter