Clinical Research Associate II - Oncology (Ohio/Kentucky)
AbbVie · Ohio City, OH
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Role summary
AbbVie seeks a Clinical Research Associate II for oncology studies in Ohio/Kentucky to serve as the primary site contact, oversee trial conduct and data integrity, and mentor less experienced staff. The role ensures protocol compliance, patient safety, and effective site engagement throughout clinical trial execution.
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 Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.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
- Health-related tertiary qualification (medical, scientific, or nursing preferred)
- Minimum 1 year clinically related experience with 6 months in clinical research monitoring
- Knowledge of risk-based monitoring approaches for investigational drug or device trials
- Advanced understanding of ICH/GCP guidelines and local regulatory requirements
- Strong cross-functional collaboration and interpersonal skills with excellent communication abilities
- Demonstrated planning, organizational skills and proficiency with clinical trial technology tools
- Ability to apply critical thinking and clinical judgment to resolve site-level issues
What you'll be doing
- Serve as primary contact for investigative sites, providing contextual trial information and strengthening stakeholder connections
- Conduct site evaluations, training, routine monitoring and closure activities in compliance with protocols and GCP standards
- Develop and customize site engagement strategies using CRM tools to track progress and measure impact
- Mentor and train less experienced CRAs on clinical trial aspects and contribute to their professional development
- Identify risk signals proactively, ensure audit and regulatory inspection readiness, and manage corrective action plans
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.