Key Responsibilities:
- Leads statistical programming activities for one or more compounds/indications or a therapeutic area.
- Ensures timely deliverables, that all quality processes are followed, and consistency within projects.
- Develops and oversees SAS programs for the creation of ADaM data sets following CDISC standards.
- Develops and oversees SAS programs for the creation of Tables, Listings and Figures.
- Ensures consistency of ADaM data sets for individual studies and integrated data.
Qualifications:
- Education/Experience: MS in Statistics, Computer Science, Chemistry, or related science field.
- 6 years of experience as a SAS/Statistical Programmer with:
- Conducting statistical programming in SAS related to drug development.
- Developing SAS programs following CDISC standards.
- Creating documentation for regulatory filings.
- 2 years of experience leading a team of statistical programmers.
Benefits:
- Salary range: $190,683.90 - $230,000.00 per year.
- Paid time off (vacation, holidays, sick), medical/dental/vision insurance, 401(k) (eligible employees).
- Eligible to participate in short-term and long-term incentive programs.
Application Instructions:
- Apply online: https://careers.abbvie.com/en
- Or send resume to: Job.opportunity.abbvie@abbvie.com
- Refer to Req ID: REF49727J