Drive clinical study success locally with AstraZeneca as a Clinical Research Associate. Lead monitoring efforts, ensure compliance, and engage actively with study sites to enhance trial outcomes.
As a Clinical Research Associate (CRA), you will manage study site activities from initiation to closure. Collaborating closely with local study teams, your role is pivotal in adhering to ICH-GCP guidelines and AstraZeneca's protocols. You will also contribute to investigator training and oversee regulatory compliance for all assigned studies.
Key Responsibilities:
• Monitor study sites to ensure proper study conduct
• Prepare and close clinical sites under AZ procedural documents
• Train site staff in regulatory and study-related requirements
• Conduct regular monitoring visits and audits
• Ensure timely resolution of study-related issues
Requirements:
• Bachelor's degree in life science or related field
• Strong knowledge of ICH-GCP and local regulations
• Ex...