Clinical site monitoring and regulatory expertise drive this AbbVie Clinical Research Associate II position, supporting Phase I to III studies. Travel is at least 50%.

As a Clinical Research Associate II, you monitor investigative sites and anticipate study-related issues. The work spans site qualification, initiation, interim monitoring, and closeout visits. You apply Good Clinical Practice, ICH Guidelines, and AbbVie Standard Operating Procedures while supporting protocol execution and study quality.

Key Responsibilities:

- Monitor clinical investigative sites for protocol execution and compliance
- Conduct qualification, initiation, interim monitoring, and closeout visits
- Manage corrective action plans and inspection readiness
- Verify timely,



accurate safety and study data submissions
- Train site personnel on protocols and regulatory requirements

Requirements:

- Health-related tertiary qualification preferred
- Minimum two years of clinical monitoring experience
- In office investigational drug or device trial experience required
- In-depth knowledge of clinical research regulations and ICH/GCP
- Valid driver’s license, passport, and willingness to travel

Apply clinical monitoring, regulatory knowledge, and clear communication to advance AbbVie studies while protecting participants and maintaining quality.

📌 Clinical Research Associate Site Monitoring (Oakville)
🏢 AbbVie
📍 Oakville