Elevate your career as a Clinical Research Associate II with AbbVie.

Your role will involve managing clinical investigations while proficiently ensuring compliance with all regulatory standards. Bring your clinical monitoring skills to AbbVie, where the focus is on cutting-edge R&D; across various therapeutic areas. In this position, you will conduct quality site visits, guarantee adherence to protocols, and maintain study data integrity through effective monitoring plans. Key Responsibilities:
Oversee clinical site activities to ensure compliance
Conduct Phase I to III study site visits
Motivate site personnel towards meeting objectives
Assure quality and timely safety data submissions
Support training for site personnel on study protocols Requirements:
Minimum of 2 years in clinical monitoring
In-depth knowledge of ICH/GCP guidelines
Solid analytical and interpersonal skills
Experience with clinical research technologies
Willingness to travel at least 50% Make a meaningful impact in clinical research with AbbVie, promoting patient safety and data accuracy.

📌 Abbvie Clinical Research Associate Role Edmonton
🏢 Allergan
📍 Edmonton