Clinical Research Associate I – Immunology

AbbVie

. Advance AbbVie’s clinical research pipeline by supporting excellence in clinical research .

Posted 10/26/2026full-timeRemote • Florida • United StatesJuniorMid-Level💰 $75,000 - $142,500 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical research coordination, ensuring compliance with ICH/GCP Guidelines and local regulatory requirements while effectively managing site relationships and training staff. Leverages critical thinking and organizational skills to enhance recruitment strategies and maintain audit readiness.

Highest-signal resume keywords

Clinical Research CoordinationICH/GCP Guidelines KnowledgeSite Relationship ManagementRegulatory ComplianceCritical Thinking

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementData ManagementSite EvaluationMonitoring PlansRisk AssessmentPatient Recruitment TechniquesSafety-Event ReportingAudit ReadinessTherapeutic-Area KnowledgeRegulatory Inspection Readiness

Soft Skills

CollaborationPlanningOrganizational SkillsCommunication SkillsSelf-Motivation

Tools & Technologies

CRM Tools

Industry Keywords

Clinical ResearchInvestigative SitesGCP ComplianceICH GuidelinesHealth-Related Discipline

About the role

Key responsibilities & impact

Advance AbbVie’s clinical research pipeline by supporting excellence in clinical research
Serve as the primary point of contact for investigative sites
Provide clinical-trial context and connect stakeholders with investigative sites
Align, train, and motivate site staff and principal investigators under supervision
Conduct site evaluation, training, routine monitoring, and site closure activities under supervision
Ensure compliance with protocols, monitoring plans, regulations, GCPs, ICH Guidelines, SOPs, and quality standards
Customize site engagement strategies and track progress using CRM tools
Connect study protocols, scientific principles, and clinical-trial requirements to daily execution
Evaluate recruitment and retention techniques based on the patient disease journey
Develop therapeutic-area, asset, clinical-landscape, and patient-journey knowledge
Perform continuous risk assessment with the Central Monitoring team
Resolve site risk signals and implement preventative and corrective action plans
Identify, evaluate, and recommend investigators and sites under supervision
Ensure quality and timely submission of site data and safety-event reporting
Maintain audit and regulatory inspection readiness
Manage investigator payments according to executed contract obligations, as applicable

Requirements

What you’ll need

Appropriate tertiary qualification in a health-related discipline (Medical, Scientific, Nursing) preferred, or equivalent work experience
Clinically related experience, preferably in clinical research coordinating or data management
Knowledge of therapeutic-area indications preferred
Knowledge of local regulatory and legal requirements, ICH/GCP Guidelines, and applicable policies
Ability to work collaboratively and cross-functionally
Planning and organizational skills; ability to manage competing projects and deadlines
Ability to leverage technology, tools, and resources
Critical thinking and good judgment for addressing clinical site issues
Strong written, verbal, active listening, and presentation skills
Ability to establish and leverage site relationships through engagement, motivation, and training
Integrity consistent with AbbVie’s code of business conduct and leadership values
Self-motivated, focused on timely and quality outcomes
Ability to work remotely

Benefits

Comp & perks

Paid time off (vacation, holidays, sick)
Medical, dental, and vision insurance
401(k)
Eligibility to participate in long-term incentive programs
Equal opportunity employment
Reasonable accommodation for US and Puerto Rico applicants