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Key Responsibilities
Qualifications :
Education & Experience
Must have a BS in Statistics Computer Science or a related field & 5 years of statistical programming experience. Of the experience required must have: (i) 5 years utilizing SAS programming concepts & techniques related to drug development & regulatory filings; (ii) 5 years applying CDISC standards including ADaM & Study Data Tabulation Model (SDTM); (iii) 5 years developing SAS programs for the creation of ADaM data sets following CDISC standards & for the creation of Tables Listing & Figures; (iv) 3 years working in a matrixed organization working across business stakeholders & line functions to gather analyze synthesize requirements & translate; (v) 2 years developing standard SAS macros; & (vi) 1 year providing oversight & mentoring of assigned Statistical Programmers & Statistical Analysts. Alternatively will accept a Masters degree in Statistics Computer Science or a related field & 2 years of statistical programming experience. Of experience required must have: 2 years of experience with (i) through (iii); 1 year of experience with (iv) & (v); & 6 months of experience with (vi).
Experience may be gained concurrently. Any suitable combination of education & work experience will be acceptable.
100% telecommuting allowed.
Additional Information :
Salary Range: $160000 $197000 per year
Apply online at Refer to Req ID: REF39459F.
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 shortterm and longterm 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.
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No
Employment Type :
Fulltime
Full-time