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New · posted Nov 1

Abbott · Medical Devices

Clinical Research Associate

  • Remote, US
  • Remote
  • Full-time
  • Associate & Specialist
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EmploymentFull-time
LocationRemote, US
DeadlineOpen until filled

The role

Our Core Lab business unit currently has an opportunity for a Clinical Research Associate. This role is based remote in the United States near a major airport or in an Abbott Office approved.

Our diagnostic solutions are used in hospitals, laboratories, and clinics around the globe. The crucial information derived from our tests, instruments, and informatics systems is often the first step in patient care decision-making for hundreds of health conditions from heart attacks to blood disorders to infectious diseases and cancers.

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.

What you need

Required Qualifications

  • Bachelor's (life sciences or clinical research preferred) or equivalent combination of education and work experience.
  • Minimum 1-year clinical research experience required.
  • Must be detail-oriented and efficient in time management.
  • Must have excellent written and verbal communication, organizational and presentation skills.
  • Must be able to work effectively with others.
  • Self-directed and able to work within a fast paced and constantly changing environment.
  • Ability to multitask, prioritize, and manage time efficiently.
  • Proficient computer skills, including Microsoft Office Suite (Word, Excel, Outlook, etc.).
  • Travel: 40 %

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: https://abbottbenefits.com/

What you'll do

What You’ll Work On

As a Clinical Research Associate (CRA), you will support clinical trial sites from study start-up through closeout, ensuring studies are conducted in compliance with protocols, regulatory requirements, and company procedures.

This role reports to the Clinical Manager and partners with Clinical Project Teams and Operations leadership. The successful candidate will work in a regulated quality environment, manage assigned tasks and timelines, build cross-functional relationships, and contribute to study success under general supervision.

  • Conduct site qualification, initiation, monitoring, and closeout visits.
  • Provide training and support to investigators, study coordinators, and site staff.
  • Monitor protocol compliance, data quality, and Good Clinical Practice (GCP) requirements.
  • Review source documents and verify clinical study data for accuracy and completeness.
  • Ensure only eligible participants are enrolled in studies.
  • Manage and maintain study and regulatory documentation.
  • Monitor investigational product accountability and inventory.
  • Review adverse event reporting for accuracy and compliance.
  • Assess site performance, including patient recruitment and retention efforts.
  • Prepare monitoring reports and communicate findings, risks, and corrective actions.
  • Build strong relationships with clinical research sites and internal stakeholders.
  • Develop knowledge of applicable clinical research regulations and study types.

Pay and benefits

$61,300 – $122,700 a year

Employer provided
How this compares

The base pay for this position is

$61,300.00 – $122,700.00

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

  • Free medical coverage through Health Investment Plan (HIP) PPO

  • Retirement savings plan with high employer contribution

  • Tuition reimbursement

  • Freedom 2 Save student debt program

  • FreeU education benefit

  • Career development

Working conditions

Standard

TRAVEL

Yes, 50 % of the Time

MEDICAL SURVEILLANCE

Yes

JOB FAMILY

Medical & Scientific Affairs

DIVISION

CRLB Core Lab

LOCATION

United States > California : Remote

ADDITIONAL LOCATIONS

United States of America : Remote

Smiling Abbott colleagues in Abbott T-shirts packing disaster relief boxes together

From the posting

About Abbott

Working at Abbott

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.
Abbott company page · 108 open roles
Equal opportunity, accessibility and legal noticesAbbott's statements, word for word

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.

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), Continuous walking for prolonged periods (more than 2 hours at a time in an 8 hour day), Driving a personal auto or company car or truck, or a powered piece of material handling equipment, Keyboard use (greater or equal to 50% of the workday), Lift, carry, push or pull weights of more than 20 pounds/9 kilos on a regular/daily basis, Work with human blood or other potentially infectious materials, Work with infectious organisms or known infectious materialsAbbott 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

Job intelligence

The context around this role

Live data · November 1, 2026

Salary intelligence

How the pay compares

This role's midpoint is 16% below the US median for Clinical Research roles at this level.

This roleEmployer provided

$61,300 to $122,700 a year

Associate & Specialist roles in California9 roles publishing pay

Middle half $102,500 to $130,500, median $111,500

Associate & Specialist roles in the US56 roles publishing pay

Middle half $80,000 to $127,875, median $110,000
Annual base pay
Annual base payLowMedianHigh
This role$61,300—$122,700
California$102,500$111,500$130,500
All US$80,000$110,000$127,875

This role: Abbott's own published range. Comparisons: the base pay employers published on open Clinical Research roles at the same level on Regulatory Jobs, November 1, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Clinical Research

The general path across 193 open Clinical Research roles on Regulatory Jobs, with the titles they carry most. Not Abbott's own promotion track.

  1. This role

    Associate & Specialist

    Often: Clinical Research Associate · Clinical Research Coordinator

    $110K median102 open
  2. Next step

    Senior & Principal

    Often: Senior Clinical Research Associate · Sr. CRA

    $125K median87 open
  3. Later

    Manager

    Often: Associate Clinical Research Manager · Senior Clinical Research Manager

  4. Later

    Director

    Often: Associate Director, Site Monitoring · Director, Clinical Trial Liaison

Skills DNA

What this role leans on

How many of the posting's 28 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 4 linesLab testing and methods: 1 lineDocumentation and SOPs: 5 linesInvestigations and CAPA: 2 linesValidation and qualification: 1 lineData and digital systems: 1 lineClinical trial conduct: 10 linesCollaboration and leadership: 6 linesGMPLab testingDocumentationInvestigationsValidationData systemsClinical trialsTeamwork
  • Clinical trial conduct10
  • Collaboration and leadership6
  • Documentation and SOPs5
  • GMP and compliance4
  • Investigations and CAPA2
  • Lab testing and methods1
  • Validation and qualification1
  • Data and digital systems1

Regulatory intelligence

The rules behind this role

Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.

Company hiring pulse

Abbott on Regulatory Jobs

108
Open roles
98
Distinct roles
32
Locations

By discipline

  • Quality61 56%
  • Regulatory30 28%
  • Clinical16 15%

By level

  • Senior & Principal50 46%
  • Associate & Specialist33 31%
  • Manager21 19%
See all 108 Abbott roles

More roles at Abbott

All 108 Abbott roles

Similar Clinical Research roles elsewhere

Clinical Research Associate at Abbott

Open until filled. $61K–$123K a year, employer provided.

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