Embark on a 12-month journey with AstraZeneca as a Biopharma Study Management Operations Intern. This pivotal role involves supporting clinical studies while balancing remote and in-office collaboration three days a week.
Based in Mississauga, the intern will aid the Global Study Associate Directors and Managers in executing clinical studies throughout their lifecycle. Key responsibilities include managing the electronic Trial Master File and ensuring compliance with regulatory guidelines, as well as crafting clinical regulatory documents for submission. This role is perfect for candidates seeking to gain hands-on experience in clinical trial management.
Key Responsibilities:
• Support clinical study execution and documentation
• Manage set-up and maintenance of the electronic Trial Master File




• Prepare and handle clinical regulatory documents
• Coordinate study materials, supplies, and logistics
• Assist in administrative tasks for audits and inspections
Requirements:
• Educational background in medical or biological sciences
• Strong organizational and analytical skills
• Previous administrative experience preferred
• Computer proficiency for daily tasks
• Understanding of the Clinical Study Process
Contribute to creative clinical studies while developing essential skills at AstraZeneca in Mississauga.
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📌 Biopharma Study Operations Intern at AstraZeneca (Toronto)
🏢 AstraZeneca
📍 Toronto