Associate Principal Scientist, Stat. Programming - A&r Standards, Innovation (hybrid)

Merck & Co., Inc.

Unknown, US
Base: $142,400.00 - $224,100.00; bonus/equity: ann...
Hybrid (3 days onsite, 1 day remote)
9 years sas programming experience
Cdisc sdtm and adam standards knowledge
Clinical trial programming expertise
Merck & Co., Inc. is seeking an Associate Principal Scientist in Statistical Programming, primarily responsible for developing global programming standards for drug and vaccine projects. The position emphasizes collaboration, statistical programming expertise, and adherence to established guidelines within a hybrid work environment

Job Summary

  • This position supports the design and delivery of efficient, flexible, and modular analysis and reporting standards for drug and vaccine projects across all therapeutic areas.
  • The role requires significant expertise in developing global programming standards for ADaM datasets, efficacy analysis, and safety analysis while adhering to departmental guidelines.
  • Candidates will represent the company on industry initiatives such as R Consortium, TransCelerate, PHUSE, and CDISC while collaborating with key stakeholders.

Matching Summary

Match Score: 85

Merck & Co., Inc. is seeking an Associate Principal Scientist in Statistical Programming, primarily responsible for developing global programming standards for drug and vaccine projects. The position emphasizes collaboration, statistical programming expertise, and adherence to established guidelines within a hybrid work environment.

Salary

Base: $142,400.00 - $224,100.00; Bonus/Equity: Annual bonus and long-term incentive eligible; Benefits: Medical, dental, vision, 401(k), paid holidays, vacation

Skills & Requirements

Must-have

  • 9 years SAS programming experience
  • CDISC SDTM and ADaM standards knowledge
  • Clinical trial programming expertise

Nice-to-have

  • R and Python programming experience
  • Natural language processing experience
  • Unix/Linux environment proficiency

Key Requirements

  • BA/BS plus 9 years SAS experience OR MS plus 7 years
  • Minimum 9 years clinical trial environment experience
  • Strong project management and leadership skills

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter