Senior Manager - Statistical Programming (Remote)
Senior Manager - Statistical Programming (Remote)
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1 Vacancy
Job Description
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.
Responsibilities
- 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.
Key Stakeholders
Directors of Statistics
Data Scientists
Medical Writers
Regulatory Publishers
Clinical Project Managers
Qualifications :
*This position can be hybrid at any of our US locations or work remotely US*
Minimum Qualifications:
- 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.
Additional Information :
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.
This job is eligible to participate in our long-term incentive programs
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 & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
Yes
Employment Type :
Full-time
Employment Type
Remote
