Join AstraZeneca as a Clinical Study Management Operations Intern for a 12-month paid contract. This role combines onsite collaboration and versatile remote work to support vital clinical study processes.
Working from Mississauga, the intern will assist in the management of clinical studies, collaborating with study associates and managers to ensure timely execution. Responsibilities range from maintaining the electronic Trial Master File to interacting with internal teams and external vendors for regulatory compliance. Ideal for those interested in clinical research and project management.
Key Responsibilities:
• Assist with clinical study execution and documentation
• Oversee electronic Trial Master File maintenance
• Collaborate on regulatory documents for submission
• Coordinate logistical support for study activities
• Prepare materials for meetings and communications
Requirements:
• Background in medical or biological sciences preferred
• Proven organizational and analytical skills
• Administrative experience advantageous
• Proficient in computer applications for daily use
• Basic knowledge of the Clinical Study Process
Engage in meaningful work while gaining insights into the clinical research field at AstraZeneca.
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