Clinical Research Associate I

Abbott

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

Posted 9/17/2026full-timeRemote • Illinois • 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 site staff and investigators. Proficient in monitoring data quality and maintaining study documentation, with strong communication and organizational skills.

Highest-signal resume keywords

Clinical Research ExperienceGood Clinical Practice (GCP)Site MonitoringRegulatory ComplianceMicrosoft Office Suite

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementProtocol Compliance MonitoringData Quality VerificationSite QualificationAdverse Event ReportingStudy Documentation ManagementPatient Recruitment AssessmentTraining and SupportMonitoring Report PreparationInvestigational Product Accountability

Soft Skills

Detail-OrientedTime ManagementExcellent CommunicationOrganizational SkillsSelf-Directed

Industry Keywords

Clinical ResearchStudy Start-UpStudy CloseoutClinical ProtocolsRegulatory RequirementsClinical Research SitesStudy TypesSite PerformanceFast-Paced EnvironmentMultitasking

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
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
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 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 of 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.)
Willingness and ability to travel approximately 40% (also listed as 50% in the posting metadata)

Benefits

Comp & perks

Career development with an international company
Free medical coverage in the Health Investment Plan (HIP) PPO medical plan for qualifying employees
Excellent retirement savings plan with a high employer contribution
Tuition reimbursement
Freedom 2 Save student debt program
FreeU education benefit
Diverse career opportunities
Health and wellness benefits