Senior Statistician (Eye Care)

Irvine, CA - USA

Monthly Salary: Not Disclosed

Posted on: 30+ days ago

Vacancies: 1 Vacancy

Job Summary

Key Responsibilities

Provide expertise to design analysis & reporting of clinical trials & scientific research studies.
Independently develop protocols & statistical analysis plans (or product safety analysis plans/integrated summary of safety analysis plans/analysis plans for GMA evidence generation) with details for programming implementation.
Collaborate with Statistical Programming to ensure delivery of high-quality outputs according to agreed-upon timelines.
Develop strategy for data presentation & inference.
Work collaboratively with multifunction teams in publication of scientific research.
Ensure that study results & conclusions are scientifically sound clearly presented & consistent with statistical analyses provided.

Qualifications :

Education & Experience

Must have a PhD in Statistics Biostatistics Mathematics or a highly related field & 1 year of academic industry or research experience performing statistical data analyses.

Of experience required must have 1 year:

(i) identifying data or analytical issues & assisting with providing solutions;

(ii) using SAS &/or R statistical software.

Of experience required must have at least 1 pharmaceutical industry summer internship (10 weeks):

performing statistical data analyses; &

(ii) conducting scientific research & handling trial design analysis & reporting of scientific research in clinical trials inferential statistics causal inference or real-world analytics.

Experience may be gained concurrently.

Hybrid (onsite 3 days a week/ 2 days WFH/remote).

Additional Information :

Salary Range: $147450.37 - $178500.00 per year.

Apply online at or send resume to . Refer to Req ID: REF45975B

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 committed to operating with integrity driving innovation transforming lives serving our community and embracing diversity and inclusion. It is AbbVies policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race color religion national origin age sex (including pregnancy) physical or mental disability medical condition genetic information gender identity or expression sexual orientation marital status status as a protected veteran or any other legally protected group status.

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 & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

Employment Type :

Full-time

Key ResponsibilitiesProvide expertise to design analysis & reporting of clinical trials & scientific research studies.Independently develop protocols & statistical analysis plans (or product safety analysis plans/integrated summary of safety analysis plans/analysis plans for GMA evidence generation)...