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Summary

The Principal Statistician supports the design, execution, analysis, interpretation, and reporting or communication of data evidence for discovery, manufacturing, research, development, and/or marketed product needs with minimal supervision. The role supports statistical aspects of business-critical and/or regulatory commitments, provides input to program plans with limited supervision, and represents Statistics for cross-functional teams or working groups.

• Independent study execution experience
• Recent oncology experience (Solid tumors, hematology malignancies)
• Study start-up experience.
• Regulatory submission experience
• Experience in quality assurance for TLFs, important ADaM datasets, and endpoint derivations. Hands-on QC or validation using SAS or R.
• Strong skills in collaborating with other functions (clinical, data management, regulatory)
• Ability to operate as an independent study statistician for multiple studies.

Education and Experience Requirements

• Ph.D. in Statistics or related field with minimum 3 years relevant experience, or Master’s in Statistics or related field with minimum 5 years of relevant experience.
• Proficient in SAS or R programming.
• Good written, oral, and interpersonal communication skills.
• Ability to work independently.
• Demonstrated ability to work in interdisciplinary contexts outside statistics

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com