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Senior Clinical Scientist Jobs (NOW HIRING)

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 ...

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 ...

The Senior Clinical Research Scientist will join the Clinical Science & External Research (CSER) Team responsible for global evidence generation and dissemination of scientific findings from clinical ...

The Senior Director, Clinical Scientist provides clinical and scientific leadership for assigned oncology studies and programs. This individual serves as a key member of Study and Program Teams ...

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The Senior Director, Clinical Scientist provides clinical and scientific leadership for assigned oncology studies and programs. This individual serves as a key member of Study and Program Teams ...

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How much do senior clinical scientist jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for senior clinical scientist in the United States is $71.16, according to ZipRecruiter salary data. Most workers in this role earn between $53.12 and $79.09 per hour, depending on experience, location, and employer.

What is a senior clinical scientist?

Senior Clinical Scientists are experienced professionals who design, conduct, and manage clinical research studies to evaluate new medical treatments, drugs, or devices. They lead clinical research teams, ensure compliance with regulatory standards, analyze study data, and collaborate with cross-functional departments such as regulatory affairs and medical writing. Their work is crucial in advancing medical knowledge and bringing safe, effective products to market. Senior Clinical Scientists often mentor junior staff and play a key role in strategic planning for clinical development programs.

What are the key skills and qualifications needed to thrive as a senior clinical scientist?

To thrive as a Senior Clinical Scientist, you need advanced knowledge in clinical research, protocol development, and data analysis, typically supported by a PhD or advanced degree in a relevant scientific field. Familiarity with clinical trial management systems (CTMS), regulatory compliance tools, and good clinical practice (GCP) certification is highly valuable. Excellent leadership, problem-solving, and communication skills enable effective collaboration across cross-functional teams and stakeholders. These competencies ensure rigorous scientific standards, regulatory compliance, and successful execution of complex clinical trials.

What are the typical collaborative relationships a senior clinical scientist maintains within a clinical trial team?

Senior Clinical Scientists play a pivotal role in clinical trial teams by working closely with cross-functional partners, such as clinical project managers, data managers, medical writers, and regulatory affairs specialists. They often serve as scientific leads, ensuring protocol integrity and consistency throughout the study. Effective collaboration is essential for resolving scientific or operational issues, interpreting clinical data, and communicating findings to both internal stakeholders and external partners like investigators and CROs. This collaborative dynamic helps ensure studies are conducted efficiently and with high scientific rigor.

Do you need a PhD to be a senior clinical scientist?

A PhD is often preferred for senior clinical scientist roles, especially those involving research or complex data analysis, but it is not always mandatory. Many employers also value relevant experience, advanced degrees such as a master's, and professional certifications like the Certified Clinical Research Professional (CCRP).
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Infographic showing various Senior Clinical Scientist job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $148,012 per year, or $71.2 per hour.

Senior Clinical Scientist

Abbott

Santa Clara, CA

$100K - $200K/yr

Full-time

Medical, Retirement

Posted 21 days ago


Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 138 frontline employees who took The Breakroom Quiz

175th of 543 rated manufacturers


Job description

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.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

$100,000.00 - $200,000.00

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

JOB FAMILY:Clinical Affairs / StatisticsDIVISION:SH Structural HeartLOCATION:United States > Santa Clara : 4551 Great America ParkwayADDITIONAL LOCATIONS:United States > Minnesota > St. Paul : 1225 Old Highway 8 NWWORK SHIFT:StandardTRAVEL:Yes, 10 % of the TimeMEDICAL SURVEILLANCE:NoSIGNIFICANT 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.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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