8d ago

Staff Scientist - Real World Evidence and Data Science

2 Locationslead
Data ScienceData & AI
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Quick Summary

Overview

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,

Technical Tools
Data ScienceData & AI
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 122,000 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 

 

For years, Abbott’s medical device businesses have offered technologies that are faster, more effective, and less invasive. Whether it’s glucose monitoring system, innovative therapies for treating heart disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives better and healthier. Every day, our technologies help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks. 

 

The Opportunity 

 

Our location in Santa Clara, CA currently has an on-site opportunity for a Staff Clinical Research Scientist. This new team member will work in Abbott’s Global Data Science & Analytics team within the Medical Device Division. The Staff Clinical Research Scientist will provide scientific and technical leadership for real‑world evidence (RWE) studies supporting post‑market regulatory requirements, reimbursement, market development, and pre-market submissions across Abbott’s Vascular portfolio. This individual will lead the design, execution, and dissemination of observational studies using large‑scale real‑world data sources, including electronic health records (EHR), insurance claims, hospital administrative and billing databases, and device‑generated data. The Staff Clinical Research Scientist will collaborate with thought leaders within the organization and outside the company, developing creative ways to present key findings to the research community. 

 

 

What You’ll Work On  

 

Requirements

~3 min read
  • Masters Degree (± 18 years), Preferred 

  • Minimum 9 years, Related work experience with a complete understanding of specified functional area. 

  • Comprehensive knowledge and application business concepts, procedures and practices. Uses in-depth knowledge of business unit functions and cross group dependencies/ relationships. Is recognized as an expert in work group. Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations.; 3. (Cognitive Skills) Works on complex problems where analysis of situations or data requires an in-depth evaluation of various factors. Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results. Has broad knowledge of various technical alternatives and their potential impact on the business. 

 

Preferred Qualifications 

  • PhD, DrPH, MS, or equivalent advanced degree in epidemiology, biostatistics, clinical research, public health, outcomes research, biomedical engineering, or a related discipline. 

  • 4–8 years of experience in real‑world evidence, observational research, outcomes research, or related analytical research roles in industry, academia, consulting, or government. 

  • Hands‑on experience working with real‑world data sources, such as electronic health records, administrative claims data, hospital billing data, registries, or similar large healthcare datasets. 

  • Deep knowledge in observational study design and epidemiologic methods, including cohort studies, definition of exposures and outcomes, confounding considerations, and sensitivity analyses. 

  • Experience in development of RWE study protocols, analysis plans, or study reports, with exposure to regulatory or post‑market evidence needs considered a plus. 

  • Practical experience performing data analysis and programming using one or more of the following: SQL, R, SAS, Python, or similar statistical/analytical languages. 

  • Experience collaborating with data analysts to validate analytical datasets, programs, and study outputs. 

  • Experience in development of study reports, abstracts, slide decks, and manuscripts, with mentorship as needed. 

  • Familiarity with regulatory or methodological guidance relevant to RWE or observational studies, with the ability to apply guidance under supervision. 

  • Background or interest in the coronary or peripheral vascular space or a related cardiovascular therapeutic area (e.g., structural heart, heart failure, rhythm management), with willingness and ability to build domain expertise over time. 

  • Demonstrated ability to manage multiple projects or workstreams simultaneously, prioritize tasks effectively, and deliver high‑quality work under timelines, with strong attention to detail. 

  • Excellent written and verbal communication skills, with the ability to explain analytical concepts and results clearly to cross‑functional partners and proven ability to publish scientific manuscripts 

  • Experience working in cross‑functional team environments, including collaboration with clinical, regulatory, medical affairs, or health economics, is preferred. 

     

$114,000.00 – $228,000.00

In specific locations, the pay range may vary from the range posted.

     

Clinical Affairs / Statistics

     

MD Medical Devices

        

United States > Santa Clara : Building A - SC

     

United States > Sylmar : 15900 Valley View Court

     

Standard

     

Yes, 10 % of the Time

     

Yes

     

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)

     

Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.

     

EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf

     

EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

Location & Eligibility

Where is the job
—
Location terms not specified
Who can apply
Same as job location

Listing Details

Posted
October 5, 2026
First seen
October 5, 2026
Last seen
October 11, 2026

Posting Health

Days active
7
Repost count
0
Trust Level
32%
Scored at
October 13, 2026

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Staff Scientist - Real World Evidence and Data Science