Senior Manager Statistical Programming
- Employer
- Eisai Inc.
- Location
- Nutley, New Jersey
- Start date
- Nov 4, 2024
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- Discipline
- Information Technology, Bioinformatics
- Required Education
- Masters Degree/MBA
- Position Type
- Full time
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At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai’s human health care (hhc) mission. We’re a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer’s disease. As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile, we want to hear from you.
Job Summary
Responsible for SAS programming activities supporting multiple studies for a single, or multiple compounds within related therapeutic areas. Programming experience from inception through submission in related areas.
Essential Functions
- Develop code to create datasets to facilitate the analysis specified in the Statistical Analysis Plan. 15%
- Develop code to create summary Tables, Graphs, and Listings (TLGs) to summarize the data according the Statistical Analysis Plan. 15%
- Develop code to verify the accuracy of the Datasets created by other programmers or by the CRO. 15%
- Develop code to verify the accuracy of the results of the summary Tables, Graphs, and Listings created by other programmers or by the CRO. 15%
- Answer questions from the CRO regarding the study analysis. 15%
- Participate in study team meetings. 15%
- Represent Biostats and programming in cross-function meetings. 10%
Requirements
- MS degree with a minimum of 6 years proven pharma industry experience in clinical development statistical programming methods & processes is required.
- In depth experience as a statistical programmer within the clinical development function of a therapeutic area(s). Ability to effectively follow instructions and work under supervision.
- Functioning primarily as an individual contributor, it is also expected that he/she will at times work with vendors and therefore must have good communication skills.
- Experience with CDISC (SDTM/ADaM) is also required.
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