Coordinate clinical research sites from Mississauga in a hybrid Site Management Associate role using documentation and vendor communication skills.
This Site Management Associate I role supports clinical research activities across sites, vendors, and study teams. You will coordinate supplies, submissions, payments, audits, queries, EDC completion, and site communications. The position also supports training, document management, safety information flow, CTMS updates, and vendor tracking.
Key Responsibilities:
- Exchange study information and documentation with sites and vendors
- Coordinate clinical supply orders, inventory, distribution, returns, and reconciliation
- Support regulatory and ethics committee submissions and notifications
- Maintain site files, TMF documents, translations, and tracking systems
- Update CTMS and track site issues, actions, and deadlines
Requirements:
- College or university degree, or equivalent education, training, and experience
- Minimum two years of clinical research or administrative experience
- Basic proficiency in Microsoft Word, Excel, Outlook, and PowerPoint
- Proficiency in English and basic English typing skills
- Knowledge of applicable software following proper training
Apply clinical research administration, site coordination, documentation, and systems skills across this hybrid Mississauga position.
Clinical Research Site Management Associate in Mississauga employer: PSI CRO
At PSI, we pride ourselves on being an exceptional employer, offering a collaborative work culture that fosters innovation and professional growth. As a Clinical Project Management Lead, you will benefit from our commitment to employee development, competitive compensation, and the opportunity to make a meaningful impact in clinical research across North America. Join us in a dynamic environment where your leadership will drive success and contribute to advancements in healthcare.
