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
• Robust 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.
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📌 Abbvie Clinical Research Associate Role Edmonton (Canada)
🏢 Allergan
📍 Canada