Job Description
Become a vital part of clinical trials at Novo Nordisk, supporting operations from start-up through close-out in a remote role. Bring your expertise in compliance and documentation management.
As a Clinical Trial Associate, you'll manage intricate details of clinical trials while ensuring quality and compliance across all phases. Your responsibilities span from supporting document collection for Regulatory Authorities to coordinating trial logistics. This role is perfect for those with a keen eye for detail and strong organizational abilities.
Key Responsibilities:
• Provide administrative support across all clinical trial phases
• Manage electronic Trial Master Files for compliance
• Coordinate clinical supply and equipment activities
• Facilitate document submissions to authorities
• Support meeting logistics and follow-ups
Requirements:
• Bachelor’s degree in life sciences or related field
• Preferred experience in pharmaceutical or CRO environments
...
As a Clinical Trial Associate, you'll manage intricate details of clinical trials while ensuring quality and compliance across all phases. Your responsibilities span from supporting document collection for Regulatory Authorities to coordinating trial logistics. This role is perfect for those with a keen eye for detail and strong organizational abilities.
Key Responsibilities:
• Provide administrative support across all clinical trial phases
• Manage electronic Trial Master Files for compliance
• Coordinate clinical supply and equipment activities
• Facilitate document submissions to authorities
• Support meeting logistics and follow-ups
Requirements:
• Bachelor’s degree in life sciences or related field
• Preferred experience in pharmaceutical or CRO environments
...
Ready to Apply?
Submit your application today and join our talented team at Novo Nordisk, Inc..
Submit ApplicationJob Details
- Location toronto, on
- Job Type Full-time
- Category Other-General
- Posted Date June 04, 2026
- Application Deadline July 14, 2026