Associate Principal Scientist, Statistical Programming, Late-Stage Oncology (Hybrid)
$142.4k - $224.1kMerck
Associate Principal Scientist role leading statistical programming for late-stage oncology clinical trials and regulatory submissions. Responsible for developing analysis datasets, coordinating global programming teams, and serving as the statistical programming lead across the product lifecycle.
Responsibilities
- Develop, validate, and maintain statistical analysis and reporting deliverables including datasets, tables, listings, and figures for clinical trials and regulatory submissions
- Design and manage statistical datasets supporting clinical development, outcomes research, and safety evaluation across multiple stakeholder groups
- Lead and coordinate global programming teams including outsource providers; manage project plans and resource forecasting
- Serve as statistical programming point of contact and knowledge holder for assigned projects throughout the product lifecycle
- Participate in departmental strategic initiatives and ensure adherence to departmental SOPs and programming best practices
Requirements
- BA/BS in Statistics, Computer Science, Applied Mathematics, or related field plus 9+ years SAS programming in clinical trials; or MS in related field plus 7+ years experience
- Advanced SAS expertise including data steps, procedures, macros, and graphics with database systems knowledge
- Experience with CDISC and ADaM standards for clinical data
- Knowledge of clinical data management and ability to comprehend statistical analysis plans
- US and/or worldwide regulatory submission experience including electronic submission deliverables
- Strong interpersonal, written, and presentation skills with ability to lead complex projects
- Experience with quality assurance, process compliance, and cross-functional stakeholder collaboration
Vacancy posted 21 days ago
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