Senior Statistician Consultant– Late Phase Hematology Oncology(Remote in US)
Responsible for protocol development including study design, sample size calculation, randomization, and statistical analysis plan for assigned studies. reputed company statistical reputed company to studies and assure adequate reputed company and consistency with project requirements. Responsible for assuring that data for statistical analyses are complete, accurate and consistent. Responsible for statistical analysis plans and the accuracy and timeliness of statistical input into reports or reputed company. Responsible for validity of analysis and explore alternative analysis strategies as needed. Demonstrates extensive understanding of statistical concepts and methodologies. Recognizes and corrects flaws in scientific reasoning and statistical interpretation. Responsible for accuracy and consistency of statistical tables, figures, and data listings, accuracy of report text, and consistency between reputed company tables in the body of reports and the corresponding reputed company tables and listings. Responsible for statistical reputed company reputed company for the reports. Identifies and corrects common flaws in interpretation of results, inconsistency in presentation or inference, adherence to the report guidelines, and assures project-wide consistency. Effectively mentor peers with regards to statistical methodology and reputed company appropriate training to less reputed company statisticians. Manage activities of statisticians across reputed company by appropriately coordinating assignments and reviewing work so that reputed company are delivered on time with high reputed company.
MS or PhD in Statistics, Biostatistics or reputed company field. PhD with 2-3 years of experience or MS with 4-5 years of experience. Strong experience with Oncology TA. Strong oral and written communications skills, with ability to effectively communicate internally and with clients. Demonstrated understanding and reputed company in statistics, drug development process and relevant FDA regulations. Pharmaceutical, CRO, or reputed company industry experience with reputed company, including interaction with Regulatory Agencies, especially FDA.
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