Coordinate clinical trial site activation remotely, using regulatory documentation expertise and accurate investigator site communication. Support studies from startup through conduct.

As a Site Activation Partner, you will manage essential documents and operational activities across clinical studies. You will prepare submissions, support IRB workflows, maintain committee activities, and coordinate with investigators, study teams, and stakeholders. The work includes activation, ongoing documentation, and site compliance.

Key Responsibilities:

- Coordinate startup activities and compile Investigator Initiation Packages
- Prepare and submit regulatory documents for internal approval
- Support local IRB submissions from preparation through approval




- Maintain study documents, systems, and Trial Master Files
- Resolve site issues and support audit responses

Requirements:

- Minimum two years clinical site management experience
- Knowledge of clinical trial methodologies and ICH-GCP
- Understanding of FDA and local country regulations
- Fluency in local language and English
- Life sciences education preferred

Apply clinical research knowledge, regulatory coordination, and site management skills across global clinical trial activation and conduct.

📌 Clinical Trial Site Activation Partner (Montreal)
🏢 Parexel
📍 Montreal