Shape the future of clinical trials with Ocugen as a Clinical Research Associate. Oversee Phase 1-3 studies while ensuring participant safety and data integrity in a dynamic environment.

This Canada-based position is integral to the clinical research team, handling the planning, start-up, execution, oversight, and closeout of clinical studies. As a Clinical Research Associate, you will coordinate site activities, maintain essential documentation, and collaborate with CROs to ensure compliance with ICH Good Clinical Practice standards. A robust background in clinical research and relevant education is essential for success.

Key Responsibilities:
• Support start-up, execution, and closeout of clinical trials
• Coordinate site identification, qualification, and training




• Oversee monitoring and quality assurance activities
• Maintain accurate study trackers and documentation
• Manage investigational product tracking and related activities

Requirements:
• Bachelor’s degree in life sciences, nursing, or pharmacy
• At least three years of clinical research experience
• Familiarity with eTMF, CTMS, and EDC systems
• Knowledge of ICH GCP and regulatory requirements
• Strong organizational and problem-solving abilities

Drive excellence in clinical study management through meticulous oversight and collaboration at Ocugen.
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📌 Clinical Research Associate at Ocugen (Ontario)
🏢 OCUGEN OPCO
📍 Ontario