Објавено во: Останато во Калифорнија | Последни промени: |
Job Description
Key Responsibilities
Develop statistical methodology for protocols with details for programming implementation.
Provide expertise for design, analysis & reporting of clinical trials & other scientific research studies. Implement statistical methodology in scientific investigations.
Identify scientifically appropriate data collection instruments.
Identify & report data issues or violations of study assumptions.
Provide programming specifications for derived variables & analysis datasets.
Perform statistical computations & simulations as per the analysis plan to ensure the delivery of high-quality outputs according to agreed-upon timelines.
Identify & anticipate issues arising in the study design as well as conduct & propose scientifically sound approaches.
Evaluate appropriateness of available software for planned analyses & assess needs for potential development of novel statistical methodology.
Utilize experience with Statistical Analysis System (SAS®) software, R software, & familiarity with software tools for designing statistically optimized clinical trials.
Develop strategy for data presentation & inference.
Collaborate in publication of scientific research.
Ensure accuracy and internal consistency of reports & publications, including tables, listings, & figures.
Ensure that study results & conclusions are scientifically sound, clearly presented, & consistent with statistical analyses provided.
Work collaboratively with multifunctional teams & provide responses to questions, & pursue analyses suggested by data.
Support communications between assigned product teams & functional management.
