Offer summary
Qualifications:
Bachelor's degree in clinical research or equivalent experience, Experience in project administration and clinical research, Specialized graduate diploma in drug development is an asset, Excellent English communication skills; French is a plus, Proficient in Word, Excel, and PowerPoint.
Key responsabilities:
- Support site activation activities during clinical trial lifecycle
- Prepare and manage essential regulatory documents
- Establish and coordinate timelines for site activation
- Communicate with sites and escalate concerns to the Project Manager
- Assist with training, document management, and site correspondence