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Senior Clinical Scientist

Abbott · IL · Remote available · $86,700–$173,300 a year · Full time

Posted Sep 11, 2026 · We last checked this listing on Oct 6, 2026

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Likely interview questions for this role

Written from this job description, not a generic list. Each one notes what the interviewer is really checking.

About your past

Tell me about a clinical study report or publication you wrote. What was hardest about it?

What they are checking: Whether they can write clear, defensible scientific documents.

How do you work with biostatisticians when you disagree on an analysis approach?

What they are checking: Whether they can debate methods respectfully and reach a sound decision.

How do you stay current on the structural heart literature and competitor trials?

What they are checking: Whether they have a real habit of tracking the field.

Describe a time you explained complex clinical data to a non-scientific audience such as marketing or leadership.

What they are checking: Whether they can translate science for business decisions without losing accuracy.

What would you do

An investigator wants to publish a subgroup result that looks exciting but was not prespecified. How do you respond?

What they are checking: Whether they protect scientific integrity and explain the limits of post hoc findings.

About the work

This role is in the Structural Heart division. What do you know about clinical evidence needs for structural heart devices like transcatheter valves or repair systems?

What they are checking: Whether they understand the clinical field and the kinds of endpoints these trials use.

Walk me through how you would contribute to a clinical protocol, including endpoints, inclusion criteria and sample size thinking.

What they are checking: Whether they can design a scientifically sound study that also works in practice at sites.

How do you review clinical data for safety signals during an ongoing device study?

What they are checking: Whether they can spot meaningful trends and know when to escalate.

How would you support a regulatory submission with clinical content, such as for a PMA?

What they are checking: Whether they understand what regulators need from the clinical section and how to present it.

How do you handle adverse event adjudication or clinical events committee work?

What they are checking: Whether they understand how independent event review protects study credibility.

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The full job description

As published by Abbott.

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. JOB DESCRIPTION: At Abbott, you can do work that matters, grow, and learn, care for yourself and your 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 a 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 worldwide 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 the best place to work for diversity, working mothers, female executives, and scientists. The Opportunity This position is part of our Structural Heart Division. Our business purpose is to restore health and improve quality of life by designing and providing device and management solutions for treating structural heart disease. As the Senior Clinical Scientist, you'll have the chance to be responsible for the design, execution, and monitoring of internal and external clinical studies. What You’ll Work On • Develops and/or reviews departmental operating procedures. • Develops study protocols for executing experiments, evaluation, and documentation of results. • Follows standard and complex procedures in executing studies, evaluation, and documentation of results. • Participates in the development of clinical strategy for the product development. • Responsible for the design, execution and monitoring of Abbott sponsored external clinical studies including PMA and outcome studies. • Responsible for identification and qualification of external clinical sites. • Responsible for the development and maintaining of operating procedures. • Participates in the development of clinical strategy to support product development and market introduction. • Participates in cross functional team activities for product development including risk management. • Successful and timely completion of clinical studies directly impacts the ability to meet product development goals and product introduction timelines. Required Qualifications • Bachelors Degree (± 16 years) In a related field and/or an equivalent combination of education and work experience. • Minimum 8 years in conducting clinical studies or related laboratory skills. Preferred Qualifications • Experience in medical device related studies is desirable. • Knowledge of regulations governing medical devices is desirable. • Experience conducting medical device clinical trials preferred (TAVR in particular). • Investigational Device Exemption (IDE) trial experience. • Physician management. • Safety management desirable. • Experience working with external clinical research committees (i.e. screening committees, DSMB, CEC). Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com 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 The base pay for this position is $86,700.00 – $173,300.00 In specific locations, the pay range may vary from the range posted. JOB FAMILY: Clinical Affairs / Statistics DIVISION: SH Structural Heart LOCATION: United States of America : Remote ADDITIONAL LOCATIONS: WORK SHIFT: Standard TRAVEL: Yes, 10 % of the Time MEDICAL SURVEILLANCE: No SIGNIFICANT WORK ACTIVITIES: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday) 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

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