Tasks:

• Lead study startup in Canada, including updating study documents (e.g., Informed Consent Form ) to align with Canadian regulatory and EC requirements.
• Compile and manage submission packages for Health Canada and EC approvals.
• Handle contract negotiations with sites, including serving as the primary point of contact.
• Support site management during startup, ensuring timely SIV preparation and execution.
• If budget is secured post-SIV, tr...