Abbott Posted September 24, 2026

Senior Clinical Research Scientist

Alameda, California, United States FULL_TIME
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Abbott is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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.

The Opportunity:

Organize and conduct, or participate in, all performance evaluations for new products, product enhancements, and product process changes. Participate as the clinical resource on product development teams, working with R&D, Regulatory Affairs, Quality Assurance and Marketing in identifying user needs and market segments, and presenting relevant evaluation results as necessary.

What you’ll do:

Provide clinical knowledge and expertise in clinical study protocol development, clinical trial design, analysis and interpretation

Solid performance in creating high quality, scientifically sound and medically accurate documents that are clear and focused for clinical research and regulatory agency submissions (such as FDA).

Expertise with health care and medical communication and effective use of on-line research databases, such as Pubmed, and use of integrated referencing software.

Evaluates new product ideas and business opportunities by reviewing pertinent literature and other available information, summarizing information and making recommendations to appropriate departments.

Scientific review and input to CRF development. Excellent collaboration skills with biostatistics and data management.

Participates in the Risk Analysis process for new or improved devices to ensure that potential risks to patients associated with use of the device and risks to study execution are identified and appropriately analyzed.

Creates clinical performance evaluation plans to assess physician acceptance and the expected performance of new products by interacting with appropriate personnel, (e.g., physicians, engineers, other clinical coordinators, regulatory affairs).

Cultivates relationships with internal and external customers, (e.g., consultants and investigators) to continue to grow their expertise in clinical research.

Writes device Instructions for Use (IFU).

Provide clinical knowledge, expertise and direction relevant to manufacturing, quality, performance and patient safety during all phases of development of a product or concepts to ensure informed decisions are made in these areas.

Support product development by contributing clinical knowledge to bench testing, performing in-vitro and /or in-vivo device evaluations and assisting in the development of new test methods to provide a better understanding of device performance.

Coordinate and conduct post-market clinical evaluations of new product designs or enhancements.

Participates in Product Action process by performing and documenting a Health Risk Assessment and communicating the assessment to Quality Assurance.

Required Qualifications:

Bachelor’s Degree in Biological Science or similar with a minimum of 9 years of related work experience with a complete understanding of specified functional area.  Master’s Degree is preferred.

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.

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.

The base pay for this position is $114,000.00 – $228,000.00. In specific locations, the pay range may vary from the range posted.

Job details

Seniority
Senior
Function
Clinical Research
Therapeutic area
Not listed
Location
Alameda, California, United States
Employment type
FULL_TIME

How this role compares

Computed from every other active Clinical Research role in our database, not just this employer's listings.

We currently track 59 comparable Senior Clinical Research roles across 6 biopharma companies.

59Comparable roles tracked
58Currently active
6Companies hiring similar roles
24Countries represented

Salary context

11 of 59 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · CRA 2/Senior CRA 1 · IQVIA $76,300/yr – $175,100/yr
Peer group range $125,700 – $203,000 (median $132,650)

Where these roles are based

Top locations among the 59 comparable roles

United States11
China7
United Kingdom6
Canada6
Netherlands3
Brazil3

+ 18 more countries

Seniority mix

59 of 59 peers have a known seniority level

Senior52
Principal6
Associate Director1

Therapeutic area mix

2 of 59 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology2

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
IQVIA Durham, United States Senior
Same function Same seniority Same country
60%similar
IQVIA Durham, United States Senior
Same function Same seniority Same country
60%similar
IQVIA Durham, United States Senior
Same function Same seniority Same country
60%similar
IQVIA Durham, United States Senior
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60%similar
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Same function Same seniority Same country

Open in 2 locations

Carlsbad, United StatesDurham, United States
60%similar
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Same function Same seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
(Senior) Clinical Research Associate
IQVIA · Durham, United States · Senior
Function Therapeutic area Seniority Country
60%
Sr. CRA, Oncology, IQVIA Biotech
IQVIA · Durham, United States · Senior
Function Therapeutic area Seniority Country
60%
Senior Clinical Research Associate, Sponsor Dedicated
IQVIA · Carlsbad, United States · Senior
Function Therapeutic area Seniority Country
60%
Senior Clinical Research Associate, Early Clinical Development
IQVIA · Durham, United States · Senior
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.