Lead clinical research projects from a home-based setting with occasional travel, using project management and regulatory compliance expertise. Coordinate teams and deliverables.

Alimentiv seeks a detail-oriented Clinical Project Manager to plan, execute, monitor, and complete clinical research studies. You will coordinate cross-functional activities, manage timelines, budgets, and documentation. The role supports patient safety, quality standards, sponsor relationships, and successful project delivery.

Key Responsibilities:

- Lead clinical research planning, execution, monitoring, and completion
- Coordinate teams across monitoring, data, statistics, and reporting
- Oversee budgets, regulatory requirements, patient safety, and operations
- Maintain protocols, SOPs, consent forms, CRFs, and study records




- Serve as primary sponsor and client contact

Requirements:

- Bachelor's degree in Health Sciences, Clinical Research, or related field
- One to three years of clinical study management experience
- Understanding of clinical research processes and regulatory requirements
- Excellent project management, organization, communication, and problem-solving skills
- Fluent English and occasional travel availability

Bring clinical study coordination, regulatory knowledge, and stakeholder communication skills to meaningful gastrointestinal research at Alimentiv.

📌 Clinical Research Project Manager (Toronto)
🏢 Alimentiv
📍 Toronto