Manage clinical study delivery for Alimentiv, coordinating sponsors, clients, investigators, and interdisciplinary teams from a home-based workplace with occasional travel. This Clinical Project Manager role combines operational planning, communication, documentation, and issue resolution across clinical research projects. You will maintain effective sponsor relationships while monitoring project objectives, deliverable quality, timelines, and regulatory alignment. The work supports Alimentiv's gastrointestinal focus and scientific research mission.

Key Responsibilities
- Manage project objectives, timelines, deliverables, and expectations
- Resolve project issues and maintain sponsor communication
- Facilitate meetings and provide regular status reports
- Monitor compliance with regulations, guidelines,



policies, and standards
- Coordinate data collection, adverse events, and study reporting

Requirements:
- Bachelor's degree in Health Sciences or related field
- One to three years' clinical research coordination experience
- Solid written and verbal English communication skills
- Exceptional attention to detail and accuracy
- Self-motivated, results-oriented, and adaptable to evolving requirements Use organized clinical study leadership, problem-solving, and communication skills to deliver compliant projects supporting Alimentiv's gastrointestinal research.

📌 Clinical Study Delivery Manager (Toronto)
🏢 Alimentiv
📍 Toronto