Coordinate clinical research project support from a home-based setting, using solid communication and organizational skills. Help teams manage meetings, training, documents, and queries.
As a Clinical Research Project Support Coordinator, you will assist project teams and stakeholders throughout the project life cycle. Responsibilities include preparing meeting materials, scheduling committees, coordinating sponsor and site meetings, tracking training, and supporting communications. You will also help maintain project forms, reports, processes, and records.
Key Responsibilities: Schedule project committees, sponsor meetings, and site meetings
Prepare agendas, minutes, presentations, and meeting documents
Track training programs and activities throughout projects
Assist with forms, reports, logs, scripts,



and information entry
Support project forms, documents, processes, and audit activities
Requirements: Minimum one to three years of related work experience
Ongoing training or relevant one-year college advanced diploma
Relevant degree in health or life sciences preferred
Knowledge of clinical research and effective communication
Ability to work independently in a cross-functional environment
Bring clinical research knowledge and reliable project coordination to meetings, training, documentation, and stakeholder support activities.

#J-18808-Ljbffr

📌 Clinical Research Project Support Coordinator (New Brunswick)
🏢 Alimentiv
📍 New Brunswick