Clinical Research Associate

Abbott

. Support clinical trial sites from study start-up through closeout .

Posted 10/16/2026full-timeRemote • California • United StatesJuniorMid-Level💰 $61,300 - $122,700 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial management, including site qualification, monitoring, and compliance with Good Clinical Practice. Proficient in data accuracy verification and regulatory documentation management while fostering strong relationships with clinical research sites and stakeholders.

Highest-signal resume keywords

Clinical Research ExperienceGood Clinical Practice ComplianceSite Monitoring and ManagementData Quality VerificationMicrosoft Office Suite Proficiency

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementSite QualificationProtocol Compliance MonitoringData Accuracy VerificationRegulatory Documentation ManagementAdverse Event ReportingPatient Recruitment AssessmentMonitoring Report PreparationInvestigational Product AccountabilityStudy Coordination

Soft Skills

Detail-OrientedTime ManagementWritten CommunicationVerbal CommunicationOrganizational Skills

Industry Keywords

Clinical ResearchStudy Start-UpSite InitiationSite CloseoutClinical Trial SitesStudy TypesClinical Manager ReportingStakeholder CommunicationFast-Paced EnvironmentMultitasking

About the role

Key responsibilities & impact

Support clinical trial sites from study start-up through closeout
Conduct site qualification, initiation, monitoring, and closeout visits
Train and support investigators, study coordinators, and site staff
Monitor protocol compliance, data quality, and Good Clinical Practice requirements
Review source documents and verify clinical study data accuracy and completeness
Ensure only eligible participants are enrolled
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
Prepare monitoring reports and communicate findings, risks, and corrective actions
Build relationships with clinical research sites and internal stakeholders
Develop knowledge of applicable clinical research regulations and study types
Report to the Clinical Manager and partner with Clinical Project Teams and Operations leadership

Requirements

What you’ll need

Bachelor's degree in life sciences or clinical research preferred, or equivalent combination of education and work experience
Minimum 1-year clinical research experience required
Detail-oriented and efficient in time management
Excellent written and verbal communication, organizational, and presentation skills
Ability to work effectively with others
Self-directed and able to work in 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.)
Ability to travel approximately 40–50% of the time
Based remotely in the United States near a major airport or in an Abbott-approved office

Benefits

Comp & perks

Career development with an international company
Free medical coverage eligibility through the Health Investment Plan (HIP) PPO medical plan
Retirement savings plan with a high employer contribution
Tuition reimbursement
Freedom 2 Save student debt program
FreeU education benefit toward a bachelor’s degree
Health and wellness benefits
Equal Opportunity Employer committed to employee diversity