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, ensuring compliance with protocols and regulatory requirements while effectively supporting clinical research sites. Proficient in monitoring data quality, conducting site visits, and managing study documentation.

Highest-signal resume keywords

Clinical Research ExperienceProtocol Compliance MonitoringGood Clinical Practice KnowledgeMicrosoft Office Suite ProficiencyTime Management Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementSite QualificationData VerificationAdverse Event ReportingStudy Documentation ManagementPatient Recruitment AssessmentMonitoring Report PreparationRegulatory ComplianceInvestigational Product AccountabilityStudy Closeout Procedures

Soft Skills

Detail-OrientedExcellent Communication SkillsOrganizational SkillsSelf-DirectedAbility to Multitask

Industry Keywords

Clinical ResearchRegulatory RequirementsGood Clinical PracticeStudy Start-UpSite MonitoringClinical Trial ProtocolsInvestigators TrainingStudy Coordinators SupportPatient RetentionQuality Environment

About the role

Key responsibilities & impact

Support clinical trial sites from study start-up through closeout
Ensure studies comply with protocols, regulatory requirements, and company procedures
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
Manage assigned tasks and timelines and contribute to study success under general supervision
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, or equivalent combination of education and work experience
Minimum 1 year of clinical research experience
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 40% / travel listed as 50% of the time
Ability to work in a regulated quality environment
Ability to work with human blood or other potentially infectious materials and infectious organisms or known infectious materials
Ability to lift, carry, push, or pull weights over 20 pounds/9 kilos on a regular/daily basis

Benefits

Comp & perks

Career development with an international company
Free medical coverage eligibility through the Health Investment Plan (HIP) PPO medical plan in the next calendar year
Retirement savings plan with a high employer contribution
Tuition reimbursement
Freedom 2 Save student debt program
FreeU education benefit toward a bachelor’s degree
Diverse career opportunities
Health and wellness benefits