Responsibilities Contribute to design, analysis and reporting of clinical trials or other scientific research studies. Assist with development of protocols and/or statistical analysis plans with details for programming implementation. Work under supervision to implement sound statistical methodology in scientific investigations. Identify and report data issues or violations of study assumptions. Provide programming specifications for derived variables and analysis datasets. Collaborate with Data Science in preparing for database lock. Perform statistical analyses as per the analysis plan. Collaborate with Statistical Programming to ensure the delivery of high-quality outputs according to agreed-upon timelines. Evaluate appropriateness of available software for planned analyses and assess needs for potential development of Client statistical methodology. Develop strategy for data presentation and inference. Ensure appropriate interpretation of statistical deliverables in collaboration with other functions. Ensure accuracy and internal consistency of reports, including tables, listings, and figures. Ensure the accuracy of the statistical component of scientific reports with high quality. Work collaboratively with cross-functional teams. Clearly explain statistical concepts to non-statisticians. Provide responses to questions and pursue analyses suggested by data. Support communications between assigned product team(s) and functional management. Build/drive cross-functional relationships and collaboration. Requirements PhD in Statistics with 1-3 years of experience or MS in statistics with 5-7 years of experience. Strong statistical methodology knowledge. Prior experience in Pharma industry reviewing SAP/protocol/CSR/database cleaning etc. Experience in Phase I is a plus but NOT required. Seniority level Mid-Senior level Employment type Full-time Job function Research, Analyst, and Information Technology #J-18808-Ljbffr Katalyst CRO
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