SAS+ R programmer (4+yrs)-immediate to 30days joiners

Position: SAS + R Programmer Experience: 45+ Years Mandatory Skill: Hands-on experience with R for SDTM Programming P referred Candidates: Immediate joiners or candidates who can join within 1 month Primary Responsibilities Communicates effectively with functional leadership concerning project issues (e.g. data, technical, timelines). Provides comprehensive programming support for project teams, including development of programming strategies, standards, specifications, and programmed analysis. Drives the development and implementation of innovative strategies and technologies to improve programming efficiency. Reviews key planning documents (e.g., protocol, statistical analysis plan, mock shells) to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements. Supports the development of unambiguous and robust programming specifications for programming work. Identifies opportunities for increased efficiency and consistency within Inference. Contributes to globalization, improvement and standardization of processes, standards, and tools. Qualification 4+years of experience as a statistical programmer in a clinical environment( SAS+ RProgramming) Significant knowledge of SAS software (i.e. Base, Stat, Graph components) and general computing as relates to clinical drug development. Graduate degree , certification from SAS preferred. Knowledge of other software (e.g. R) desired. Knowledge of the drug development process, clinical trial methodology, statistics and familiarity with global regulatory requirements Ability to work successfully within cross-functional teams Ability to be flexible and adapt quickly to the changing needs of the organization. Ability to organize multiple work assignments and establish priorities. Excellent verbal and written communications skills Position: SAS + R Programmer Experience: 45+ Years Mandatory Skill: Hands-on experience with R for SDTM Programming P referred Candidates: Immediate joiners or candidates who can join within 1 month Primary Responsibilities Communicates effectively with functional leadership concerning project issues (e.g. data, technical, timelines). Provides comprehensive programming support for project teams, including development of programming strategies, standards, specifications, and programmed analysis. Drives the development and implementation of innovative strategies and technologies to improve programming efficiency. Reviews key planning documents (e.g., protocol, statistical analysis plan, mock shells) to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements. Supports the development of unambiguous and robust programming specifications for programming work. Identifies opportunities for increased efficiency and consistency within Inference. Contributes to globalization, improvement and standardization of processes, standards, and tools. Qualification 4+years of experience as a statistical programmer in a clinical environment( SAS+ RProgramming) Significant knowledge of SAS software (i.e. Base, Stat, Graph components) and general computing as relates to clinical drug development. Graduate degree , certification from SAS preferred. Knowledge of other software (e.g. R) desired. Knowledge of the drug development process, clinical trial methodology, statistics and familiarity with global regulatory requirements Ability to work successfully within cross-functional teams Ability to be flexible and adapt quickly to the changing needs of the organization. Ability to organize multiple work assignments and establish priorities. Excellent verbal and written communications skills