Senior Statistical Analyst (Eye Care - Aesthetics)
One-Click ApplyFull-timeOn-site1mo ago30+ days old, may be filled
Clinical TrialsComplianceData AnalysisDocumentationHTMLSAS
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Responsibilities
- Deliver statistical programming expertise for clinical studies with lower complexity.
- Ensure accurate data analysis, reporting, & adherence to regulatory standards.
- Develop SAS programs for generating ADaM datasets, tables, listings, & figures.
- Create specifications for ADaM datasets for individual & integrated analyses.
- Collaborate closely with crossfunctional teams to achieve project objectives.
- Prepare documentation for regulatory submissions, including reviewers guides & data definition documents.
- Lead development of standard SAS macros & participate in development of standard operating procedures.
- Provide supervision & mentorship to statistical programmers & analysts.
- Education & Experience
- Must have a MS in statistics, biostatistics, computer science, mechanical engineering or a related field & 2 years as a statistical analyst leading statistical programming activities for clinical studies.
- Of experience required, must have 2 years:
- applying SAS programming concepts & techniques related to drug development;
- creating & validating ADaM datasets in compliance with CDISC/ADaM Standards;
- providing statistical programming supporting for Phase I, II, & III clinical trials;
- generating clinical outputs (tables, listings, & figures) with SAS; &
- utilizing each of the following SAS tools: SAS/BASE, SAS/MACROS, SAS/SQL, SAS/GRAPH, & SAS/STAT.
- Alternatively, would accept a BS in statistics, biostatistics, Computer science, mechanical engineering or a related field & 5 years as a statistical analyst leading statistical programming activities for clinical studies.
- Of experience required, must have 5 years:
- applying SAS programming concepts & techniques related to drug development;
- creating & validating ADaM datasets in compliance with CDISC/ADaM Standards;
- providing statistical programming supporting for Phase I, II, & III clinical trials;
- generating clinical outputs (tables, listings, & figures) with SAS; &
- utilizing each of the following SAS tools: SAS/BASE, SAS/MACROS, SAS/SQL, SAS/GRAPH, & SAS/STAT.
- Work experience may be gained concurrently. Will accept reasonable combination of education, training & experience.
- Salary Range: $146,467.84 - $183,500.00 per year.
- Apply online at https://careers.abbvie.com/en or send resume to Job.opportunity.abbvie@abbvie.com . Refer to Req ID: REF49786C.
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- 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 and 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 https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
- US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
- https://www.abbvie.com/join-us/reasonable-accommodations.html
Benefits
Dental insuranceVision insurance401(k)Paid time off
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