Associate Director / Director, Statistical Programming

Posted 2024-10-17

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💎 Seniority level: Director, 8+ years (director level 12+)

📍 Location: Cambridge, MA

🔍 Industry: Pharmaceuticals / Oncology

🏢 Company: Nuvalent, Inc.

🗣️ Languages: English

⏳ Experience: 8+ years (director level 12+)

🪄 Skills: LeadershipProject ManagementPeople ManagementSAS EGProject CoordinationCross-functional Team LeadershipCommunication SkillsAnalytical SkillsCollaboration

Requirements:

Master’s Degree in statistics, mathematics, computer science, or a related scientific/medical field.
8+ years of SAS statistical programming experience in clinical trials.
Advanced SAS programming skills, including Macro language and reporting.
Knowledge of CDISC SDTM and ADaM model standards.
Familiarity with regulatory guidelines related to clinical trials.
Experience with outsourcing programming activities and CRO management.
Advanced understanding of statistical concepts.

Responsibilities:

Function as lead programmer to produce and/or validate tables, listings, figures, and analysis datasets.
Write specifications for programming needs.
Develop/review TFL shells, SDTM and ADaM specifications.
Ensure the accuracy of final databases, analyses, and reports.
Partner with or oversee CROs for programming tasks.
Manage project timelines and schedules.
Identify problems and enhance efficiency through global tools.

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