Clinical Research Associate

North Chicago, ILFull-time

Behavioral Health Market Context

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•Identifies, evaluates and recommends new/potential investigators/sites on an on going basis

•Monitors activities conducted by clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol
•Conducts site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, and AbbVie Standard Operating Procedures (SOPs) and business processes
•Ensures regulatory inspection readiness at assigned clinical sites
•Ensures safety and protection of study subjects through compliance with the study monitoring plan, AbbVie SOPs, ICH Guidelines, and applicable regulations
•1 more items(s)