Associate Principal Scientist, Statistical Programming

Merck & Co., Inc.

Rahway, NJ, USA
Base: $142,400.00 - $224,100.00; bonus/equity: ann...
Hybrid (3 days onsite, 1 day remote)
Sas programming expertise
Clinical trial data manipulation
Pk/pd data integration
Merck & Co., Inc. is seeking an Associate Principal Scientist in Statistical Programming to support global PK modeling and simulation in the oncology therapeutic area. The ideal candidate will have extensive experience in SAS programming within clinical trials and strong project management skills

Job Summary

  • The role involves providing high-quality statistical programming analysis and reporting deliverables for global PK modeling and simulation stakeholders in the Oncology therapeutic area.
  • Candidates must possess significant expertise in SAS, clinical trial programming, and the ability to design complex algorithms for manipulating pharmacokinetic and efficacy data.
  • The position offers a comprehensive benefits package including medical, dental, vision, 401(k), and eligibility for annual bonuses and long-term incentives.

Matching Summary

Match Score: 85

Merck & Co., Inc. is seeking an Associate Principal Scientist in Statistical Programming to support global PK modeling and simulation in the oncology therapeutic area. The ideal candidate will have extensive experience in SAS programming within clinical trials and strong project management skills.

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

  • SAS programming expertise
  • Clinical trial data manipulation
  • PK/PD data integration
  • Modeling-ready dataset creation
  • Regulatory submission deliverables

Nice-to-have

  • Leadership of team members
  • Process improvement activities
  • Exploratory environment experience
  • Stakeholder collaboration skills
  • Project management capabilities

Key Requirements

  • Bachelor's degree plus 9 years SAS experience OR Master's plus 7 years
  • Experience in clinical trial environment
  • Knowledge of pharmaceutical development processes

Work Rights

Not specified

Tailored Resume

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