Clinical Research Associate II

📋 Description

• Monitors activities conducted by clinical investigative sites as they relate to AbbVie clinical
• Conducts site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4
• Overviews the overall activities of site personnel over whom there is no direct authority and
• Ensures quality of data submitted from study sites and assures timely submission of data, including
• Ensures safety and protection of study subjects through compliance with the study monitoring plan
• Trains study site personnel on the protocol and applicable regulatory requirements in collaboration

🎯 Requirements

• Appropriate tertiary qualification, health related (e.g., Medical, Scientific, Nursing) preferred.
• Minimum of 1 year of clinically-related experience, of which a period of 6 months is preferable in
• Fluent in English, both written and verbal.
• Current in-depth knowledge and understanding of appropriate therapeutic indications as they relate
• Current in-depth knowledge of regulations governing clinical research, ICH/GCP Guidelines and
• Strong planning and organizational skills and the ability to work effectively and efficiently in a