Clinical Research Associate II

AbbVie

. Serve as the primary point of contact for investigative sites .

Posted 9/22/2026full-timeRemote • Illinois • United StatesJuniorMid-Level💰 $84,500 - $162,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial management, including site evaluation, training, and compliance with ICH/GCP Guidelines. Possesses strong knowledge of therapeutic areas and the ability to implement effective site engagement strategies.

Highest-signal resume keywords

Clinical Research MonitoringICH/GCP GuidelinesSite Evaluation and TrainingCross-Functional CollaborationRisk-Based Monitoring

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementSite Closure ActivitiesRegulatory CompliancePatient Recruitment TechniquesData Submission and ReportingTherapeutic Area KnowledgeRisk AssessmentMonitoring TechniquesSite Engagement StrategiesInvestigator Evaluation

Soft Skills

Interpersonal SkillsOrganizational SkillsCritical ThinkingActive ListeningPresentation Skills

Tools & Technologies

CRM ToolsMonitoring Software

Industry Keywords

Clinical TrialsInvestigational Drug TrialsHealth Related DisciplinesRegulatory Inspection ReadinessQuality Standards

About the role

Key responsibilities & impact

Serve as the primary point of contact for investigative sites
Provide contextual information on clinical trials and connect stakeholders with investigative sites
Align, train, and motivate site staff and principal investigators on clinical trial goals, protocols, and patient treatment principles
Conduct site evaluation, training, routine monitoring, and site closure activities in compliance with protocols, regulations, GCPs, ICH Guidelines, SOPs, and quality standards
Customize site engagement strategies and gather local/site insights
Use CRM tools to report and track progress and measure strategy impact
Connect study protocols, scientific principles, and clinical trial requirements to daily trial execution
Evaluate recruitment and retention techniques based on the patient disease journey
Develop therapeutic area, asset, clinical landscape, and patient journey knowledge
Mentor and train less experienced CRAs
Participate in global/local task forces and initiatives
Conduct continuous risk assessment with the Central Monitoring team
Resolve site risk signals and implement preventative and corrective action plans
Identify and evaluate potential investigators and sites
Ensure quality and timely submission of site data and safety-event reporting
Maintain audit and regulatory inspection readiness
Manage investigator payments according to executed contracts

Requirements

What you’ll need

Appropriate tertiary qualification in health related disciplines (Medical, Scientific, Nursing) preferred
Minimum of 1 year of clinically related experience
At least 6 months of clinical research monitoring experience for investigational drug or device trials
Familiarity with risk-based monitoring, onsite and offsite monitoring
Knowledge of therapeutic area indications preferred
Advanced knowledge of local regulatory and legal requirements, ICH/GCP Guidelines, and applicable policies
Strong cross-functional collaboration, planning, organizational, interpersonal, written, verbal, active listening, and presentation skills
Ability to leverage technology, tools, and resources
Ability to apply critical thinking and good judgment to address clinical site issues
Integrity in accordance with AbbVie code of business conduct and leadership values
Self-motivated and able to deliver timely, quality outcomes in a fast-paced environment

Benefits

Comp & perks

Paid time off including vacation, holidays, and sick leave
Medical, dental, and vision insurance
401(k)
Short-term incentive programs
Remote work option
Equal opportunity employer benefits for veterans and disabled applicants