Associate Statistical Analyst (on-site)
Abbott · United States - California - Santa Clara ·
- Experience
- 1+ years
- Company size
- 1000+
- Salary
- USD 77,600 – 126,700 / year
Provide statistical support for Abbott Medical Devices' cardiovascular clinical studies, including QC and validation of tables/listings/figures, SAS programming, and CRF review — on-site in Santa Clara, CA.
JOB DESCRIPTION:
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
Apply Now
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
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The base pay for this position is
$77,600.00 – $126,700.00In specific locations, the pay range may vary from the range posted.