Explore a pivotal prospect as a Clinical Research Associate at Ocugen. Drive clinical projects while ensuring compliance with protocols and enhancing participant safety.

In this role, you will play a critical part in overseeing the execution and closeout of assigned clinical studies. Your responsibilities will include coordinating with investigational sites, managing data resolutions, and monitoring compliance with GCP regulations. This position combines operational oversight and quality assurance in a fast-evolving biotechnology environment.

Key Responsibilities:
• Support execution of Phase 1-3 clinical trials
• Assist with site qualification and study documentation
• Collaborate with CROs and monitor study performance
• Ensure compliance with all applicable regulations
• Prepare and maintain essential documents and records

Requirements:
• Bachelor’s in life sciences or a related field
• Minimum of three years clinical research experience
• Knowledge of ICH GCP guidelines
• Experience with eTMF and CTMS preferred
• Proven ability to manage multiple priorities

Leverage your expertise in clinical research management with Ocugen for impactful clinical trials.
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📌 Clinical Research Associate Role at Ocugen (Ontario)
🏢 Ocugen
📍 Ontario