What AbbVie Has to Offer: Our work can鈥攁nd does鈥攈ave a tangible, lasting impact on millions of people. But it鈥檚 not just the results that matter. How we achieve them matters, too. Leading with purpose, we work to build a more sustainable future for generations to come. We do that by putting our expertise, resources and talent to work to make a real difference for patients, communities and our world.
Job Type
Job Details
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 鈥� immunology, oncology, neuroscience, and eye care 鈥� and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at聽. Follow @abbvie on聽,听,听,听,听听补苍诲听.
Purpose
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
- 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.
*This position will be required to sit on-site 3 days / week*
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.
Key Stakeholders聽
鈥� Directors of Statistics
鈥� Data Scientists
鈥� Medical Writers
鈥� Regulatory Publishers
鈥� Clinical Project Managers
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or聽local law:聽鈥�
The compensation range described below is the range of possible base pay compensation that the Company聽believes in聽good faith it will pay for this role at the time聽of this posting based on the job grade for this position.聽Individual聽compensation paid within this range will depend on many factors including geographic location, and聽we聽may ultimately聽pay more or less than the posted range. This range may be modified in the聽future.鈥嬄燬alary: $121,000 - $230,000
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),听medical/dental/vision聽insurance and 401(k) to eligible聽employees.鈥�
This job is eligible to participate in our short-term incentive聽programs.聽鈥�
This job is eligible to participate in our long-term incentive聽programs鈥�
鈥�
Note: No amount of pay聽is considered to be聽wages or compensation until such amount is earned, vested, and聽determinable.聽The amount and availability of any bonus,听commission, incentive, benefits, or any other form of聽compensation and benefits聽that are allocable to a particular employee remains in the Company's sole and聽absolute聽discretion unless and until paid and聽may be modified at the Company鈥檚 sole and absolute discretion, consistent with聽applicable law.聽
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.鈥� Equal Opportunity Employer/Veterans/Disabled.聽
US & Puerto Rico only - to learn more, visit聽
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
Together, we break through We believe the paths we take to achieving our breakthroughs matter. At AbbVie, every one of our 50,000 employees is a... Read more