Clinical Research Associate I

AbbVie

Clinical Research Associate I for AbbVie engaging with clinical trial sites and managing research activities. Focus on data integrity and compliance in clinical trials to enhance patient outcomes.

Posted 5/27/2026full-timeRemote • Texas • 🇺🇸 United StatesJuniorMid-Level💰 $75,000 - $142,500 per yearWebsite

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

clinical research coordinatingdata managementsite evaluationsmonitoring activitiessite engagement strategiesrisk assessmentdata quality assurancesafety event submissiontherapeutic area knowledgescientific concepts application

Soft Skills

trainingmotivationcollaborationplanningorganizational skillscustomer centric supportself-motivationrelationship buildingcommunicationproblem-solving

Tools & Technologies

site engagement toolsregulatory compliance systemsdata management softwareclinical trial management systemsmonitoring toolsproject management toolscollaboration platformsdata analysis toolselectronic data capture systemsreporting tools

Certifications & Qualifications

Bachelor’s degreeICH/GCP Guidelines knowledge

Industry Keywords

clinical trialstherapeutic area indicationslocal regulatory requirementslegal requirementsclinical researchsafety eventspatient journeystakeholder engagementsite staff trainingfast-paced environment

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Provide context for clinical trials and connect stakeholders to investigative sites
Train and motivate site staff and investigators
Conduct site evaluations, training, and monitoring activities
Customize site engagement strategies for assigned studies
Gather local insights and utilize site engagement tools to measure impact
Proactively assess risks and monitor activities for study performance
Develop knowledge of therapeutic area and patient journey for recruitment
Ensure quality of data and timely submission of safety events

Requirements

What you’ll need

Bachelor’s degree or equivalent degree; health related preferred (e.g. Medical, Scientific, Nursing, Pharmacy)
Clinically related experience, preferably in clinical research coordinating or data management
Knowledge of appropriate therapeutic area indications is preferred
Ability to understand and apply scientific concepts as they relate to the conduct of clinical trials
Knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP Guidelines and applicable policies
Able to work collaboratively and cross functionally to develop and sustain working relationships
Strong planning and organizational skills
Ability to leverage technology, tools and resources to provide customer centric support
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)