Enhance clinical trial effectiveness with AstraZeneca in the role of Clinical Research Associate. Focus on site compliance, monitoring, and efficient study management in local clinical trials.
As a Clinical Research Associate, your main responsibility will be the local oversight of clinical studies. You will work alongside the Local Study Team to ensure compliance with international guidelines and AstraZeneca’s standards. This role involves liaising with investigators, training site staff, and ensuring all essential documents are inspection-ready at all times.
Key Responsibilities:
• Manage site qualification visits and regulatory submissions
• Conduct regular monitoring visits and data checks
• Address and resolve study-related issues proactively
• Prepare and maintain study documentation
• Participate in site quality risk assessments regularly
Requirements:
• Bachelor’s degree in life sciences or equivalent
• Familiarity with clinical study management an...