Clinical Research Associate I – Neurology

AbbVie

. Advance AbbVie's clinical research pipeline in neurology by supporting clinical trial execution .

Posted 10/7/2026full-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 trial execution, compliance with ICH/GCP Guidelines, and effective site management. Leverages strong communication and organizational skills to foster relationships with investigative sites and ensure quality outcomes.

Highest-signal resume keywords

Clinical Trial ExecutionICH/GCP Guidelines ComplianceSite ManagementClinical Research CoordinationRegulatory Knowledge

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ResearchData ManagementSite EvaluationRisk AssessmentPatient Recruitment TechniquesProtocol KnowledgeMonitoring PlansQuality StandardsSafety-Event ReportingAudit Readiness

Soft Skills

CollaborationCritical ThinkingOrganizational SkillsPresentation SkillsIntegrity

Tools & Technologies

CRM Tools

Industry Keywords

NeurologyTherapeutic Area IndicationsLocal Regulatory RequirementsClinical LandscapePatient Journey

About the role

Key responsibilities & impact

Advance AbbVie's clinical research pipeline in neurology by supporting clinical trial execution
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 on trial goals, protocols, and patient treatment principles
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 their impact using CRM tools
Apply protocol, scientific, and clinical-trial knowledge to day-to-day execution
Evaluate recruitment and retention techniques based on the patient disease journey
Develop therapeutic-area, asset, clinical-landscape, and patient-journey knowledge
Conduct continuous risk assessments 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

Requirements

What you’ll need

Appropriate tertiary qualification in health-related disciplines (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 to address clinical site issues
Strong written, verbal, active listening, and presentation skills
Ability to establish and leverage site relationships and trusted partnerships
Integrity in accordance with AbbVie 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)
Short-term incentive programs
Equal opportunity employer benefits for veterans and people with disabilities
Reasonable accommodation support for US and Puerto Rico applicants