Clinical Research Associate II – Southeast Territory

AbbVie

Clinical Research Associate advancing AbbVie’s pipeline by ensuring excellence in clinical research. Collaborating with site staff and investigators to enhance clinical trial performance and data integrity.

Posted 7/22/2026full-timeRemote • Florida, Louisiana, South Carolina • 🇺🇸 United StatesJuniorMid-Level💰 $84,500 - $162,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical research monitoring, including risk-based monitoring and compliance with ICH/GCP guidelines. Leverages strong interpersonal and organizational skills to enhance site engagement and ensure data integrity throughout the clinical trial process.

Highest-signal resume keywords

Clinical Research MonitoringRisk-Based MonitoringICH/GCP GuidelinesCross-Functional CollaborationData Integrity

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ResearchSite EvaluationSite TrainingData SubmissionRecruitment TechniquesRetention TechniquesRegulatory KnowledgeScientific Concepts ApplicationMonitoring PlansPatient Disease Journey

Soft Skills

Interpersonal SkillsPlanning SkillsOrganizational SkillsCritical ThinkingActive Listening

Tools & Technologies

Customer Relationship Management (CRM) Tool

Industry Keywords

Clinical TrialsInvestigational Drug TrialsInvestigational Device TrialsLocal Regulatory RequirementsLegal Requirements

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Advance AbbVie’s pipeline by striving for excellence in clinical research.
Partners with the investigator and site staff for meaningful and effective engagements.
Focus on site clinical research that ensures appropriate conduct of the trial while driving improvement in data integrity, compliance, overall study performance and customer experience.
Conducts site evaluation, site training, routine, and site closure monitoring activities with compliance to the protocol and monitoring plans.
Gather local/site insights and utilize site engagement tools such as the Customer Relationship Management (CRM) tool, to report/track progress and measure impact of that strategy.
Evaluate and ensure effective recruitment and retention techniques/plans based on the patient disease journey.
Possesses experienced level of competency to mentor and train less experienced CRAs on various aspects of work and provides input into their development.
Conduct continuous risk-assessment proactively, and in collaboration with Central Monitoring team.
Ensures quality of data submitted from study sites and assures timely submission of data.

Requirements

What you’ll need

Appropriate tertiary qualification in health related disciplines (Medical, Scientific, Nursing) preferred.
Minimum of 1 year of clinically related experience, of which a period of 6 months is required in clinical research monitoring of investigational drug or device trials.
Familiar with risk‐based monitoring approach, onsite and offsite monitoring.
Knowledge of appropriate therapeutic area indications is preferred with the ability to understand and apply scientific concepts as they relate to the conduct of clinical trials.
Advanced knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP Guidelines and applicable policies.
Demonstrate strong cross-functional collaboration skills among internal and external stakeholders.
Demonstrate strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines.
Advanced ability to leverage technology, tools and resources to provide customer centric support based on the health of the site.
Strong interpersonal skills with excellent written, verbal, active listening and presentation skills, with ability to establish and leverage site relationships and trusted partnerships through engagement, motivation, and training.
Ability to use functional expertise with appropriate guidance, leverage critical thinking skills and apply good judgement to address clinical site issues.
Acts with integrity in accordance with AbbVie code of business conduct and leadership values.
Self-motivated individual focused on delivering timely and quality outcomes in a fast-paced environment.

Benefits

Comp & perks

paid time off (vacation, holidays, sick)
medical/dental/vision insurance
401(k)
short-term incentive programs