Site Activation Specialist II supports clinical trial start-up through regulatory submissions, essential documents, and country-level quality oversight. This position is remote in Montreal, Quebec.
Syneos Health seeks a Site Activation Specialist II for client-dedicated work in Canada. The specialist manages country-level deliverables, tracks submission and approval milestones, and supports site activation across clinical trials. Responsibilities include local regulatory submissions, essential document collection, and communication with authorities and ethics committees.
Key Responsibilities: Manage country-level quality deliverables and submission timelines
Track milestones and investigate forecasted timeline delays




Prepare regulatory and ethics committee applications
Submit essential documents to the Trial Master File
Support end-to-end site activation processes
Requirements: Bachelor's degree
Understanding of Phase I-IV clinical trials and ICH GCP
Knowledge of clinical trial start-up processes
Robust organization, communication, and problem-solving skills
Fluency in French and English
Apply clinical trial start-up, regulatory submission, and site activation expertise with Syneos Health in Montreal.

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📌 Site Activation Specialist Clinical Trials (Quebec City)
🏢 Syneos Health
📍 Quebec City