Associate Principal Scientist, Statistical Programming

Merck · Rahway, NJ

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BiometricsFull-time$145k–$224kCompany career page

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Role summary

Associate Principal Scientist supporting statistical programming for late-stage clinical development projects at a pharmaceutical company. Responsible for developing analysis datasets, reports, and regulatory submissions while leading programming teams and maintaining statistical databases across multiple stakeholder groups.

What they're looking for

Bachelor's degree in Computer Science, Statistics, Applied Mathematics, or related field plus 9 years experience; or Master's degree plus 7 years experience
7+ years SAS programming experience including data steps, procedures, macros, and graphics in clinical trials
7+ years leading large or complex statistical programming projects with team coordination
7+ years designing complex programming algorithms and statistical databases
7+ years experience with CDISC, ADaM standards, and clinical data management systems
7+ years U.S. and/or worldwide regulatory submission experience at leadership level
Strong understanding of statistical terminology, models, analysis plans, and quality assurance processes

What you'll be doing

Develop and execute statistical analysis deliverables including safety and efficacy datasets, tables, listings, and figures
Design and maintain statistical datasets supporting clinical development, outcomes research, and safety evaluation
Lead and coordinate global programming teams including outsourced providers on multiple projects
Serve as statistical programming point of contact and knowledge holder throughout project lifecycle
Manage project plans, resource forecasting, and ensure timely high-quality deliverables

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