Drive clinical excellence as a Clinical Research Associate II at AbbVie. This role emphasizes the oversight of clinical site operations to ensure studies meet strict protocol standards.
Dedicated to transforming lives, AbbVie is seeking a professional with two years of monitoring experience to enhance our R&D; capabilities. You will be responsible for conducting training, managing site compliance, and safeguarding the quality of data collected throughout clinical trials.
Key Responsibilities:
• Monitor clinical study execution for protocol adherence
• Facilitate site initiation and closeout processes
• Engage site personnel to meet research goals
• Ensure updated safety reporting and compliance
• Train sites on regulatory requirements and protocols
Requirements:
• Minimum of 2 years clinical monitoring experience
• Proficient in ICH guidelines and GCPs
• Strong organizational capabilities
• Mastery of Microsoft Office tools
• Valid driver's license and passport needed
Capitalize on your clinical expertise to support AbbVie in delivering cutting-edge medical solutions to patients.
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📌 Clinical Research Associate II Position (Edmonton)
🏢 Allergan
📍 Edmonton