Apply📍 Cambridge, MA
🧭 Full-Time
🔍 Pharmaceuticals / Oncology
- 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.
- 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.
LeadershipProject ManagementPeople ManagementSAS EGProject CoordinationCross-functional Team LeadershipCommunication SkillsAnalytical SkillsCollaboration
Posted 2024-10-17
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