Elevate clinical research standards as a Partner for Clinical Site Activation, guiding all operational activities from start to finish for specified studies. Ensure sites meet timelines and regulatory standards while driving site initiations.

The role involves overseeing the compilation of Investigator Initiation Packages and managing site issues. A high school diploma or equivalent with two years of clinical trial experience will set you up for success. Familiarity with clinical trial regulations and proficiency in English and local languages enhances your support capabilities.

Key Responsibilities:
• Coordinate creation of high-quality initiation packages
• Address and manage clinical site activation issues
• Ensure compliance with study timelines and regulations




• Liaise with regulatory teams for accurate document submissions
• Keep clinical trial systems updated for performance tracking

Requirements:
• Minimum completion of high school diploma or equivalent
• 2+ years of experience in clinical trials
• Knowledge of GCP, FDA, and ICH requirements
• Prior experience in the pharmaceutical industry preferred
• Fluency in local language and English required

Bring your clinical trial expertise and communication skills to support stellar site activation.
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📌 Partner for Clinical Site Activation (Manitoba)
🏢 Parexel International
📍 Manitoba