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
- Strong 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.
Site Activation Specialist Clinical Trials in Montréal employer: Syneos Health
At Syneos Health Communications, we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. As a Remote Search Media Director, you'll enjoy the flexibility of remote work while being part of a dynamic team dedicated to driving impactful results in the pharma sector. We offer extensive employee growth opportunities, competitive benefits, and a commitment to professional development, making this an ideal place for those seeking meaningful and rewarding careers.
