As a Senior Engineer, you will enhance a diverse software portfolio by improving UIs, optimizing workflows, fixing C++ bugs, and integrating tools with AI agents.
Senior Scientist, Statistical Programming, Late-Stage Oncology (Remote)
🕒 25 days ago
📍 🇺🇸 Pennsylvania North Wales Upper Gwynedd - Remote💰 $117k - $184.2k / year🎸 Senior💻 Software Engineer💼 Full-Time
SAS ProgrammingClinical TrialsStatistical AnalysisData Management
📜 Description
- Support statistical programming activities for late-stage drug/vaccine clinical development projects.
- Lead one or more projects, ensuring timely and high-quality deliverables.
- Develop and execute statistical analysis and reporting deliverables.
- Design and maintain statistical datasets for multiple stakeholder groups.
- Collaborate with statistics and project stakeholders throughout the product lifecycle.
- Coordinate a global programming team and manage project plans.
🛠️ Requirements
- BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5+ years SAS programming experience in a clinical trial environment.
- MS in relevant field plus 3+ years SAS programming experience.
- Effective interpersonal, written, and presentation skills.
- Significant expertise in SAS and clinical trial programming.
- Familiarity with CDISC and ADaM standards.
✨ Benefits
- Comprehensive medical
- Dental
- Vision healthcare benefits
- Retirement benefits including 401(k).
- Paid holidays
- Vacation
- Sick days
Full job description
Join our BARDS team as a Senior Scientist in Statistical Programming, leading statistical analysis for late-stage oncology clinical development projects.
Description
- Support statistical programming activities for late-stage drug/vaccine clinical development projects.
- Lead one or more projects, ensuring timely and high-quality deliverables.
- Develop and execute statistical analysis and reporting deliverables.
- Design and maintain statistical datasets for multiple stakeholder groups.
- Collaborate with statistics and project stakeholders throughout the product lifecycle.
- Coordinate a global programming team and manage project plans.
Requirements
- BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5+ years SAS programming experience in a clinical trial environment.
- MS in relevant field plus 3+ years SAS programming experience.
- Effective interpersonal, written, and presentation skills.
- Significant expertise in SAS and clinical trial programming.
- Familiarity with CDISC and ADaM standards.
Benefits
- Comprehensive medical
- Dental
- Vision healthcare benefits
- Retirement benefits including 401(k).
- Paid holidays
- Vacation
- Sick days
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