Senior Clinical Research Associate

AbbVie · Budapest, Hungary

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Clinical OperationsFull timeCompany career page

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Role summary

AbbVie seeks a Senior Clinical Research Associate to oversee protocol execution and site management for clinical trials in Budapest. The role involves monitoring site activities, ensuring regulatory compliance, managing trial systems, and mentoring junior staff across assigned studies.

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 Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.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

Bachelor's degree in health-related field (medical, scientific, nursing, pharmacy preferred)
Minimum 3 years of site monitoring experience
Strong analytical and critical thinking skills for complex problem-solving
Excellent interpersonal and communication skills with flexibility and adaptability
Demonstrated planning, organizational skills, and ability to manage competing deadlines
Business ethics and integrity

What you'll be doing

Execute protocol-level deliverables including site start-up, activation, monitoring visits, and close-out activities
Maintain clinical trial management systems with current site-specific information and ensure regulatory compliance
Identify potential site issues affecting timelines and develop alternative solutions
Ensure audit and inspection readiness; prepare sites for audits and contribute to corrective action plans
Coach and mentor clinical research associates on various aspects of their work

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