Senior Clinical Statistical Analyst

2 days ago

lucknow, India beBeeStatistical Full time

As a statistical programmer, you will play a pivotal role in developing clinical trials. Your primary requirement is to possess strong expertise in SDTM, encompassing experience with oncology studies and proficiency in SAS and R programming languages.Strong SDTM expertiseOncology study experienceProficient in SAS and RAdditionally, you will need good working knowledge of ADaM and TFL programming. Expert-level SAS skills and advanced/proficient R programming skills are preferred. Familiarity with Agile ways of working and a solid understanding of CDISC standards are also beneficial.Hands-on experience with statistical analysis and reporting in clinical trialsProficient in SAS and R for statistical modelling, efficacy analysis, and data interpretationAbility to collaborate closely with programming and clinical teams in an agile setup.Some other essential aspects include: proper project management, version control, and the ability to communicate effectively with cross-functional teams. Moreover, you should be proficient in utilizing tools like JIRA, SVN, or Git for source code management. If you possess these qualities, we would love to hear from you

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    lucknow, India beBeeStatistical Full time

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    lucknow, India beBeeStatistical Full time

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    lucknow, India beBeeStatistical Full time

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    lucknow, India beBeeStatistical Full time

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