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
Solid organizational and analytical skills
Previous administrative experience preferred
Computer proficiency for daily tasks
Understanding of the Clinical Study Process Contribute to cutting-edge clinical studies while developing essential skills at AstraZeneca in Mississauga.

📌 Biopharma Study Operations Intern At Astrazeneca Toronto (Canada)
🏢 AstraZeneca
📍 Canada