Katalyst CRO
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Sr. Manager Statistical Programmer
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Katalyst CRO 1 week ago Be among the first 25 applicants Join to apply for the
Sr. Manager Statistical Programmer
role at
Katalyst CRO Get AI-powered advice on this job and more exclusive features. The Senior Manager of Statistical Programming is a leadership role which manages a team of statistical programmers in the research and development of new pharmaceutical products. The Senior Manager of Statistical Programming is responsible for leading the statistical programming activities for one or more compounds/indications or a therapeutic area. This role must effectively interface with Statistics, Data Sciences, Medical Writing, Regulatory Publishing and Development Operations. Leads the statistical programming activities for one or more compounds/indications or a therapeutic area. Manages a team of statistical programmers and the resource planning for their assigned projects. Ensures timely deliverables, that all quality processes are followed and consistency within the projects. Develops and oversees the development of SAS programs for the creation of ADaM data sets following CDISC standards. Develops and oversees the development of SAS programs for the creation of Tables, Listings and Figures. Ensures consistency of ADaM data sets for individual studies and integrated data. Creates documentation for regulatory filings including reviewers guides and data definition documents. Leads the development of standard SAS Macros and the development of standard operating procedures. Manages, mentors and creates career development plans for assigned staff. Participates in the recruitment and selection of new staff.
Scroll down to find an indepth overview of this job, and what is expected of candidates Make an application by clicking on the Apply button.
Responsibilities
The Senior Manager of Statistical Programming is a leadership role which manages a team of statistical programmers in the research and development of new pharmaceutical products. The Senior Manager of Statistical Programming is responsible for leading the statistical programming activities for one or more compounds/indications or a therapeutic area. This role must effectively interface with Statistics, Data Sciences, Medical Writing, Regulatory Publishing and Development Operations. Leads the statistical programming activities for one or more compounds/indications or a therapeutic area. Manages a team of statistical programmers and the resource planning for their assigned projects. Ensures timely deliverables, that all quality processes are followed and consistency within the projects. Develops and oversees the development of SAS programs for the creation of ADaM data sets following CDISC standards. Develops and oversees the development of SAS programs for the creation of Tables, Listings and Figures. Ensures consistency of ADaM data sets for individual studies and integrated data. Creates documentation for regulatory filings including reviewers guides and data definition documents. Leads the development of standard SAS Macros and the development of standard operating procedures. Manages, mentors and creates career development plans for assigned staff. Participates in the recruitment and selection of new staff.
Requirements:
MS in Statistics, Computer Science or a related field with 9+ years of relevant experience. OR BS in Statistics, Computer Science or a related field with 11+ years of relevant experience. Minimum of 2 years' experience leading a team of statistical programmers. In-depth understanding of SAS programming concepts and techniques related to drug development. In-depth understanding of CDISC Standards. In-depth understanding of the drug development process, including experience with regulatory filings. Ability to communicate clearly both oral and written. Ability to effectively represent the Statistical Programming Organization in cross functional teams. Ability to accurately estimate effort required for project related programming activities. Seniority level
Seniority levelEntry level Employment type
Employment typeContract Job function
Job functionInformation Technology IndustriesPharmaceutical Manufacturing Referrals increase your chances of interviewing at Katalyst CRO by 2x Get notified about new Senior Statistical Programmer jobs in
Boston, MA . Somerville, MA $97,510.40-$141,804.00 18 hours ago Cambridge, MA $147,000.00-$212,333.33 3 days ago Senior Statistical Programmer II (Remote) Boston, MA $124,600.00-$186,900.00 4 days ago Senior/Principal, Statistical Programmer Cambridge, MA $101,250.00-$170,100.00 5 days ago Boston, MA $73,000.00-$76,000.00 4 weeks ago Cambridge, MA $119,700.00-$222,300.00 1 week ago Principal or Senior Principal Preclinical Biostatistician Cambridge, MA $119,700.00-$222,300.00 3 hours ago Cambridge, MA $138,000.00-$185,000.00 1 month ago Boston, MA $119,700.00-$222,300.00 6 days ago Cambridge, MA $119,700.00-$222,300.00 6 days ago Cambridge, MA $147,000.00-$212,333.33 1 week ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
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Sr. Manager Statistical Programmer
role at
Katalyst CRO 1 week ago Be among the first 25 applicants Join to apply for the
Sr. Manager Statistical Programmer
role at
Katalyst CRO Get AI-powered advice on this job and more exclusive features. The Senior Manager of Statistical Programming is a leadership role which manages a team of statistical programmers in the research and development of new pharmaceutical products. The Senior Manager of Statistical Programming is responsible for leading the statistical programming activities for one or more compounds/indications or a therapeutic area. This role must effectively interface with Statistics, Data Sciences, Medical Writing, Regulatory Publishing and Development Operations. Leads the statistical programming activities for one or more compounds/indications or a therapeutic area. Manages a team of statistical programmers and the resource planning for their assigned projects. Ensures timely deliverables, that all quality processes are followed and consistency within the projects. Develops and oversees the development of SAS programs for the creation of ADaM data sets following CDISC standards. Develops and oversees the development of SAS programs for the creation of Tables, Listings and Figures. Ensures consistency of ADaM data sets for individual studies and integrated data. Creates documentation for regulatory filings including reviewers guides and data definition documents. Leads the development of standard SAS Macros and the development of standard operating procedures. Manages, mentors and creates career development plans for assigned staff. Participates in the recruitment and selection of new staff.
Scroll down to find an indepth overview of this job, and what is expected of candidates Make an application by clicking on the Apply button.
Responsibilities
The Senior Manager of Statistical Programming is a leadership role which manages a team of statistical programmers in the research and development of new pharmaceutical products. The Senior Manager of Statistical Programming is responsible for leading the statistical programming activities for one or more compounds/indications or a therapeutic area. This role must effectively interface with Statistics, Data Sciences, Medical Writing, Regulatory Publishing and Development Operations. Leads the statistical programming activities for one or more compounds/indications or a therapeutic area. Manages a team of statistical programmers and the resource planning for their assigned projects. Ensures timely deliverables, that all quality processes are followed and consistency within the projects. Develops and oversees the development of SAS programs for the creation of ADaM data sets following CDISC standards. Develops and oversees the development of SAS programs for the creation of Tables, Listings and Figures. Ensures consistency of ADaM data sets for individual studies and integrated data. Creates documentation for regulatory filings including reviewers guides and data definition documents. Leads the development of standard SAS Macros and the development of standard operating procedures. Manages, mentors and creates career development plans for assigned staff. Participates in the recruitment and selection of new staff.
Requirements:
MS in Statistics, Computer Science or a related field with 9+ years of relevant experience. OR BS in Statistics, Computer Science or a related field with 11+ years of relevant experience. Minimum of 2 years' experience leading a team of statistical programmers. In-depth understanding of SAS programming concepts and techniques related to drug development. In-depth understanding of CDISC Standards. In-depth understanding of the drug development process, including experience with regulatory filings. Ability to communicate clearly both oral and written. Ability to effectively represent the Statistical Programming Organization in cross functional teams. Ability to accurately estimate effort required for project related programming activities. Seniority level
Seniority levelEntry level Employment type
Employment typeContract Job function
Job functionInformation Technology IndustriesPharmaceutical Manufacturing Referrals increase your chances of interviewing at Katalyst CRO by 2x Get notified about new Senior Statistical Programmer jobs in
Boston, MA . Somerville, MA $97,510.40-$141,804.00 18 hours ago Cambridge, MA $147,000.00-$212,333.33 3 days ago Senior Statistical Programmer II (Remote) Boston, MA $124,600.00-$186,900.00 4 days ago Senior/Principal, Statistical Programmer Cambridge, MA $101,250.00-$170,100.00 5 days ago Boston, MA $73,000.00-$76,000.00 4 weeks ago Cambridge, MA $119,700.00-$222,300.00 1 week ago Principal or Senior Principal Preclinical Biostatistician Cambridge, MA $119,700.00-$222,300.00 3 hours ago Cambridge, MA $138,000.00-$185,000.00 1 month ago Boston, MA $119,700.00-$222,300.00 6 days ago Cambridge, MA $119,700.00-$222,300.00 6 days ago Cambridge, MA $147,000.00-$212,333.33 1 week ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr