Clinical Research Associate I

AbbVie · Madrid, Spain

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Clinical OperationsFull timeCompany career page

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Role summary

AbbVie seeks a Clinical Research Associate to monitor investigative sites conducting clinical trials across phases 1-4. The role ensures protocol adherence, regulatory compliance, and data quality while supporting site personnel and managing study operations.

What they're looking for

Health-related tertiary qualification (medical, scientific, or nursing); clinical trials master's degree preferred
Minimum 1 year clinically-related experience; 6 months in clinical research monitoring or study coordinator role required
On-site monitoring experience with investigational drug or device trials
In-depth knowledge of clinical research regulations, ICH/GCP guidelines, and applicable regulations
Strong planning, organizational, and analytical skills with ability to manage competing priorities
Excellent interpersonal and communication abilities with sound clinical judgment

What you'll be doing

Monitor clinical investigative sites to ensure protocol execution, regulatory adherence, and GCP compliance
Conduct site qualification, initiation, interim monitoring, and closeout visits for Phase 1-4 studies
Ensure data quality from study sites and timely submission of safety event reports
Train site personnel on protocol requirements and regulatory obligations
Manage investigator payments, negotiate agreements, and identify qualified new investigators and sites

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