Katalyst CRO
Principle Statistical Programmer
Katalyst CRO - New York, New York, us, 10261
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Principle Statistical Programmer
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Katalyst CRO . Responsibilities include: Providing quality deliverables by following corporate and departmental policies, procedures, and standards. Performing data manipulation, analysis, and reporting of clinical trial data. Creating analysis files, tables, listings, figures, and validating those files. Maintaining project tracking and validation documentation. Working effectively in a distributed team environment. Ensuring project objectives, clarity, accuracy, and completeness of programming requirements. Presenting statistical programming concepts to non-programming team members. Collaborating with cross-functional teams and managing timelines and priorities. Serving as a backup to the Principal Statistical Programmer. Requirements: 7-10+ years of statistical programming experience in the pharmaceutical/CRO industry. Strong macro development experience. PK/PD programming experience is a plus. Reviewing planning documents such as SAP, dataset specifications. Bachelor's or Master's in relevant scientific fields with 7-8+ years of experience. Extensive regulatory submission experience. Proficiency in SAS programming and analysis skills. Knowledge of drug development lifecycle and clinical trial data manipulation. Familiarity with CDISC SDTM, ADaM, and Define standards. Experience overseeing geographically diverse teams. Project management experience in drug development projects. Knowledge of SAS Graph and statistical packages. Seniority level
Mid-Senior level Employment type
Full-time Job function
Research, Analysis, and IT Industries
Biotechnology, IT Services, Education Administration This job is active and accepting applications. #J-18808-Ljbffr
Principle Statistical Programmer
role at
Katalyst CRO . Responsibilities include: Providing quality deliverables by following corporate and departmental policies, procedures, and standards. Performing data manipulation, analysis, and reporting of clinical trial data. Creating analysis files, tables, listings, figures, and validating those files. Maintaining project tracking and validation documentation. Working effectively in a distributed team environment. Ensuring project objectives, clarity, accuracy, and completeness of programming requirements. Presenting statistical programming concepts to non-programming team members. Collaborating with cross-functional teams and managing timelines and priorities. Serving as a backup to the Principal Statistical Programmer. Requirements: 7-10+ years of statistical programming experience in the pharmaceutical/CRO industry. Strong macro development experience. PK/PD programming experience is a plus. Reviewing planning documents such as SAP, dataset specifications. Bachelor's or Master's in relevant scientific fields with 7-8+ years of experience. Extensive regulatory submission experience. Proficiency in SAS programming and analysis skills. Knowledge of drug development lifecycle and clinical trial data manipulation. Familiarity with CDISC SDTM, ADaM, and Define standards. Experience overseeing geographically diverse teams. Project management experience in drug development projects. Knowledge of SAS Graph and statistical packages. Seniority level
Mid-Senior level Employment type
Full-time Job function
Research, Analysis, and IT Industries
Biotechnology, IT Services, Education Administration This job is active and accepting applications. #J-18808-Ljbffr