Revolution Medicines
Biotechnology
AssociatePrincipalStatisticalAnalyst
“Associate Principal Statistical Analyst at Revolution Medicines. Skills: Statistical Programming, Clinical trials, Regulatory submissions. Provide technical oversight of statistical programming resources. Provide mentorship to future leaders”
What You'll Achieve.
Timely delivery of analysis; Accuracy of clinical trial results
Industry & Context.
Analyze issues; Analyze problems
What They're Looking For.
Must Have
10-14 years Statistical Programming experience, BSA degree or suitable qualification, Statistical programming experience for clinical trials, Support production/verification of analysis datasets, tables, listings, and figures, Demonstrated ability to multi-task, Prioritize options, Anticipate challenges, Execute goals as team member
Nice to Have
Early or late-stage oncology clinical trials, Demonstrable record of leadership, Demonstrable record of teamwork, Thrives in collaborative team setting, Driven by desire to deploy innovative approaches, Driven by desire to deploy innovative technologies
What You'll Do.
Provide technical oversight of statistical programming resources
Provide mentorship to future leaders
Ensure quality and timely delivery of analysis
Provide solutions by analyzing issues
Ensure accuracy of clinical trial results
Ensure programming process conforms to SOPs
Manage timelines and vendors for deliverables
Comply with regulatory standards
Provide programming support for deliverables
Support Dose Committee meetings
Support Investigator Brochures
Support publications/presentations
Support US regulatory submissions
Support ex-US regulatory submissions
How You'll Work.
Team & Collaboration
Interdisciplinary team
Communication Scope
Technical guidance; Accuracy of results
Process & Methodology
Timeline management, Vendor management
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