BioSpace
Senior Manager, Statistical Programming (Remote)
BioSpace, South Chicago Heights, Illinois, United States
Senior Manager, Statistical Programming (Remote)
Posted 1 day ago. Be among the first 25 applicants.
Company Description AbbVie’s mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas—immunology, oncology, neuroscience, and eye care—while offering products and services in our Allergan Aesthetics portfolio.
Job Description The Senior Manager of Statistical Programming is a leadership role that manages a team of statistical programmers in the research and development of new pharmaceutical products. The Manager leads the statistical programming activities for one or more compounds/indications or a therapeutic area and interfaces with Statistics, Data Sciences, Medical Writing, Regulatory Publishing, and Development Operations.
Responsibilities
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 and adherence to quality processes 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 reviewer guides and data definition documents.
Leads the development of standard SAS Macros and the creation of standard operating procedures.
Manages, mentors, and creates career development plans for assigned staff.
Participates in the recruitment and selection of new staff.
This is a US-based remote position.
Qualifications
MS in Statistics, Computer Science, or a related field with 9+ years of relevant experience, OR BS 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 orally and in writing.
Ability to effectively represent the Statistical Programming Organization in cross‑functional teams.
Ability to accurately estimate effort required for project‑related programming activities.
Additional Information
The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors, including geographic location, and may ultimately be more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance, and 401(k) to eligible employees.
This job is eligible to participate in our short‑term incentive programs.
Note: No amount of pay is considered wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remain the Company’s sole and absolute discretion until paid.
AbbVie is an equal‑opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only – to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html
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Company Description AbbVie’s mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas—immunology, oncology, neuroscience, and eye care—while offering products and services in our Allergan Aesthetics portfolio.
Job Description The Senior Manager of Statistical Programming is a leadership role that manages a team of statistical programmers in the research and development of new pharmaceutical products. The Manager leads the statistical programming activities for one or more compounds/indications or a therapeutic area and interfaces with Statistics, Data Sciences, Medical Writing, Regulatory Publishing, and Development Operations.
Responsibilities
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 and adherence to quality processes 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 reviewer guides and data definition documents.
Leads the development of standard SAS Macros and the creation of standard operating procedures.
Manages, mentors, and creates career development plans for assigned staff.
Participates in the recruitment and selection of new staff.
This is a US-based remote position.
Qualifications
MS in Statistics, Computer Science, or a related field with 9+ years of relevant experience, OR BS 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 orally and in writing.
Ability to effectively represent the Statistical Programming Organization in cross‑functional teams.
Ability to accurately estimate effort required for project‑related programming activities.
Additional Information
The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors, including geographic location, and may ultimately be more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance, and 401(k) to eligible employees.
This job is eligible to participate in our short‑term incentive programs.
Note: No amount of pay is considered wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remain the Company’s sole and absolute discretion until paid.
AbbVie is an equal‑opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only – to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html
#J-18808-Ljbffr