Enhance clinical research initiatives with Ocugen as a Clinical Research Associate. Focus on managing Phase 1-3 studies while ensuring regulatory compliance and participant protection.

This role is based in Canada and plays a crucial part in overseeing the planning and execution of clinical trials. In this capacity, you will coordinate operational activities, manage site interactions, and maintain comprehensive study documentation. An in-depth understanding of clinical research guidelines and practices is vital for this position.

Key Responsibilities:
• Support all phases of clinical trial management
• Coordinate investigational site activities and training
• Maintain accurate CTMS and eTMF records




• Review study documentation for compliance and accuracy
• Track investigational products and documentation through all phases

Requirements:
• Bachelor’s degree in life sciences, nursing, or equivalent
• Three years of hands-on clinical research experience
• Familiarity with ICH, GCP, and Canadian regulations
• Proficiency with eTMF and CTMS systems preferred
• Strong problem-solving and communication skills

Leverage your expertise in clinical trials at Ocugen by ensuring protected and effective research practices.
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📌 Ocugen Clinical Research Associate Position (Ontario)
🏢 OCUGEN OPCO
📍 Ontario