Clinical Research Associate II applicants will apply clinical site monitoring expertise at AbbVie, with travel supporting Phase I to III studies. This position proactively resolves site issues and supports protocol execution across study start-up, execution, and close-out. You will monitor investigative sites, conduct visits, and communicate corrective action. The work requires knowledge of clinical research regulations, ICH/GCP Guidelines, and applicable AbbVie procedures.

Key Responsibilities
- Monitor clinical investigative sites for protocol and quality compliance
- Conduct qualification, initiation, interim monitoring, and closeout visits
- Manage site action plans and inspection readiness
- Ensure timely, accurate data and safety event reporting




- Train site personnel on protocols and regulatory requirements

Requirements:
- Health-related tertiary qualification preferred
- Minimum two years of clinically related monitoring experience
- In office investigational drug or device trial monitoring experience
- Current knowledge of ICH/GCP and clinical research regulations
- Minimum 50% travel, valid driver’s license, and passport Bring site monitoring, regulatory knowledge, and corrective-action skills to AbbVie’s clinical research studies as a Clinical Research Associate II.

📌 Clinical Research Associate II Monitoring (Vancouver)
🏢 AbbVie
📍 Vancouver