Clinical Research Associate I - Oncology (Little Rock/Shreveport/Dallas)
AbbVie · Little Rock, AR
The apply link worked recently (not employer-confirmed).
Role summary
Clinical Research Associate I position supporting oncology trials across multiple sites in the south-central region. The role focuses on site management, protocol compliance, data integrity, and ensuring patient safety while building strong relationships with investigative sites.
Where this listing comes from
This listing was compiled by RoleLantern from the employer's publicly available posting on SmartRecruiters, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-06 (originally posted 2026-10-06). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.
What they're looking for
- Tertiary qualification in medical, scientific, or nursing discipline or equivalent work experience
- Clinical research coordinating or data management experience
- Knowledge of ICH/GCP Guidelines and applicable regulatory requirements
- Understanding of scientific concepts and ability to apply them to clinical trial conduct
- Strong written, verbal, and presentation skills with active listening ability
- Planning and organizational skills with ability to work in dynamic, competing priority environments
- Collaborative cross-functional approach with integrity and self-motivation
What you'll be doing
- Serve as primary contact for investigative sites, providing trial information and strengthening partnership positioning
- Conduct site evaluations, training, monitoring activities, and closure in compliance with protocols and GCP standards
- Develop customized site engagement strategies and track progress using CRM tools and site insights
- Monitor clinical sites for study performance and patient safety issues in collaboration with central monitoring teams
- Ensure data quality, timely submission from sites, and audit/regulatory inspection readiness at assigned sites
Key requirements
- Therapeutic area
- Oncology
Privacy & handoff
This role links to AbbVie's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.