Associate Statistical Analyst (on-site)

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:

Career development with an international company where you can grow the career you dream of.

Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year

An excellent retirement savings plan with high employer contribution

Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.

A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.

A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

We are seeking an Associate Statistical Analyst to join our Clinical Research team for Abbott Medical Devices on-site in Santa Clara, CA. In this role, the Associate Statistical Analyst will provide statistical support to the Biostatistics Supervisor/Manager and the Cardiovascular Division (CVD) for clinical studies. This includes assisting

with the review of table mockups, CRFs and edit check specifications; work with biostatisticians to validate

data tables, figures and listings; write and document programs; assist in ad hoc programming; and assist in

QC.

What You’ll Work On

Assist with QC and validation of tables, listings, figures based on table specifications.

QC summary statistics in presentation slides and clinical reports against validated tables, figures, listings.

Assist with the review of CRF, edit checks, and table mock-ups and provide comments to lead statistician/ Statistical Analyst.

Independently modify existing table programs.

Assist in creating data listing or summary to Data Management for data cleaning.

Assist in documentation of programs and specification documents.

Demonstrate basic knowledge of SAS data steps, procedures and macros.

Be able to use existing macros.

Provide accurate and timely answers to routine questions.

Communicate an understanding of basic clinical principles for his/her project and acts in accordance with those principles.

Inform supervisor or manager on important issues in a timely manner.

Required Qualifications

Associate’s degree.

Minimum 1 year of experience.

Preferred Qualifications

Master’s degree or PhD

2 years’ experience in medical device or pharmaceutical clinical research studies.

Statistical knowledge and SAS skills (i.e., proven experience in SAS coding).

Experience working on medical device clinical studies in highly regulated environment.

Ability to work within a team and as an individual contributor in a fast-paced, changing environment.

Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.

Multitasks, prioritizes and meets deadlines in timely manner.

Strong organizational skills, attention to detail, and financial/business acumen

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com

Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.

The base pay for this position is $77,600.00 – $126,700.00. In specific locations, the pay range may vary from the range posted.