Statistical Programmer

4 weeks ago

Delhi, India Cytel Full time
Working under the direction of Senior Statistical Programmer/Team Lead, the

Statistical Programmer

conducts programming activities for a trial, early-phase project, indication, or publication activities.Responsibilities include:Read and understand the program specifications document.Prepare SAS analysis datasets, tables, listings, and figures as per specifications.Create programs to create graphs and tables that are required in CSRs, safety reports, efficacy reports, etc. ensuring on-time quality delivery.Validate and transform datasets as per client assignment specifications.Validate tables, listings, and figures as per client assignment specifications.Ability to work on data migration from legacy datasets to standards such as CDISC or any other client-specific standard.Coordinate with the client and US team for clarity of specifications, data issues, outliers, reviews, schedules, etc.Perform all the above tasks using standard operating procedures (SOPs) as defined in Quality Management System or the respective client(s) as applicableHands-on exposure working as a Biostatistician (writing SAP, providing statistical inputs to specs/study docs, reviewing study docs from a stats perspective)Qualifications and Experience:Masters in Sciences, with a minimum of 5 years of SAS programming experience with clinical trial data.General knowledge of regulatory requirements and drug development process.Fair knowledge of the Clinical trial domain and good SAS programming skillsAbility to work independently.Why Cytel?Our collaborative working environment encourages innovation and rewards results, and we are proud to have one of the lowest turnover rates in the industry.In addition to competitive compensation, we offer an excellent benefit's package, annual bonus incentive, promote work-life balance, and the opportunity to grow with usWork with respected experts and thought leaders.

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