Support clinical project teams from a home-based setting through document control, meeting coordination, and stakeholder communications. Keep project information organized, tracked, and aligned.

This Clinical Project Coordinator provides administrative, clerical, implementation, and processing support across project activities. The work includes document management, reporting, training coordination, billing support, and responding to project queries. Success requires clinical research knowledge, communication skills, independent work, and cross-functional collaboration.

Key Responsibilities:

- Manage and maintain project materials, tools, equipment, and supplies
- Track, update, revise, distribute, and record project activity
- Prepare forms, logs, reports, scripts, and project documents




- Support issue identification and resolution during audits
- Ensure activities follow protocols, standards, and regulatory guidelines

Requirements:

- One to three years of related work experience with training
- Relevant one-year college advanced diploma or degree
- Health, life sciences, or clinical research education preferred
- Knowledge of clinical research and robust communication skills
- Ability to work independently and cross-functionally

Apply clinical research knowledge and organized document control skills to support compliant project delivery from your home-based setting.

📌 Clinical Project Coordinator Document Control (Mississauga)
🏢 Alimentiv
📍 Mississauga