Enhance your clinical research skills as a Clinical Research Associate at Ocugen. Support diverse clinical studies while ensuring participant safety and study compliance with industry standards.

This role at Ocugen focuses on the planning, execution, and oversight of Phase 1-3 clinical trials. As a Clinical Research Associate, you will coordinate site activities, support trial management, and maintain essential documentation. You will ensure reliable data collection and participant protection in line with GCP and regulatory requirements.

Key Responsibilities:
• Oversee the start-up and closeout of clinical trials
• Coordinate site identification and essential-document collection
• Serve as the primary contact for investigational sites




• Maintain accurate study trackers and metrics
• Review monitoring reports and identify risks

Requirements:
• Bachelor’s degree in life sciences or equivalent
• At least three years in clinical research field
• Familiarity with ICH E6(R3) GCP
• Experience with eTMF and CTMS systems
• Strong organizational and problem-solving skills

Join Ocugen to advance your career in clinical research, focusing on cutting-edge trials and participant safety.
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📌 Clinical Research Associate at Ocugen (Ontario)
🏢 Ocugen
📍 Ontario