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.

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📌 Clinical Project Coordinator Document Control (British Columbia)
🏢 Alimentiv
📍 British Columbia