Join AbbVie as a Clinical Research Associate II, where you'll proactively manage clinical site studies. Leverage your monitoring expertise to ensure compliance and execution of innovative research protocols.
This role requires a minimum of two years’ experience in clinical monitoring related to investigational trials. You will conduct site activities from qualification through closeout while adhering to strict regulations and Good Clinical Practices (GCPs). Your impact will ensure data quality, regulatory readiness, and the safety of study participants.
Key Responsibilities:
• Monitor clinical sites for protocol adherence
• Conduct initiation and closeout visits for studies
• Influence site personnel to meet study objectives
• Assure timely reporting of safety events
• Train site staff on protocols and regulations
Requirements:
• 2+ years of clinical monitoring experience
• Knowledge of clinical trial regulations and GCPs
• Solid planning and organizational skills
• Proficiency in Microsoft Office Suite
• Valid driver's license and passport required
Utilize your clinical expertise to advance AbbVie’s groundbreaking research and improve patient outcomes.
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📌 Clinical Research Associate II at AbbVie (Edmonton)
🏢 Allergan
📍 Edmonton