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 . Get AI-powered advice on this job and more exclusive features. Responsibilities
Provide quality deliverables by following corporate and departmental policies, procedures, and applicable standards. Perform data manipulation, analysis, and reporting of clinical trial data. Create analysis files, tables, listings, and figures, and validate those files. Maintain project tracking and validation documentation. Work well in an environment with distributed team members. Ensure project objectives are aligned, and programming requirements are clear, accurate, and complete. Present statistical programming concepts to non-programming team members as necessary. Collaborate effectively with cross-functional teams and interface with stakeholders to manage timelines and priorities. Serve as back-up to the Principal Statistical Programmer as needed. Requirements
7-10+ years of statistical programming experience in the pharmaceutical/CRO industry. Strong macro development experience is required. PK/PD programming experience is a plus. Review planning documents (e.g., Statistical Analysis Plan, dataset specifications). BA/BSc or Master's in Statistics, Mathematics, Computer Science, Life Sciences, or related field with 7-8+ years of relevant experience. Extensive regulatory submission and response experience. In-depth SAS programming skills with excellent analysis and reporting abilities. Knowledge of drug development lifecycle and clinical data manipulation, analysis, and reporting. Thorough knowledge of CDISC SDTM, ADaM, and Define standards. Ability to oversee geographically diverse programming teams. Project management experience on drug development projects. Expertise in SAS Graph and statistical packages. Additional Details
Seniority level: Mid-Senior level Employment type: Full-time Job function: Research, Analyst, and IT Industries: Biotechnology, IT Services, Education Administration
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Principle Statistical Programmer
role at
Katalyst CRO . Get AI-powered advice on this job and more exclusive features. Responsibilities
Provide quality deliverables by following corporate and departmental policies, procedures, and applicable standards. Perform data manipulation, analysis, and reporting of clinical trial data. Create analysis files, tables, listings, and figures, and validate those files. Maintain project tracking and validation documentation. Work well in an environment with distributed team members. Ensure project objectives are aligned, and programming requirements are clear, accurate, and complete. Present statistical programming concepts to non-programming team members as necessary. Collaborate effectively with cross-functional teams and interface with stakeholders to manage timelines and priorities. Serve as back-up to the Principal Statistical Programmer as needed. Requirements
7-10+ years of statistical programming experience in the pharmaceutical/CRO industry. Strong macro development experience is required. PK/PD programming experience is a plus. Review planning documents (e.g., Statistical Analysis Plan, dataset specifications). BA/BSc or Master's in Statistics, Mathematics, Computer Science, Life Sciences, or related field with 7-8+ years of relevant experience. Extensive regulatory submission and response experience. In-depth SAS programming skills with excellent analysis and reporting abilities. Knowledge of drug development lifecycle and clinical data manipulation, analysis, and reporting. Thorough knowledge of CDISC SDTM, ADaM, and Define standards. Ability to oversee geographically diverse programming teams. Project management experience on drug development projects. Expertise in SAS Graph and statistical packages. Additional Details
Seniority level: Mid-Senior level Employment type: Full-time Job function: Research, Analyst, and IT Industries: Biotechnology, IT Services, Education Administration
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