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 • Solid problem-solving and communication skills

Leverage your expertise in clinical trials at Ocugen by ensuring safe and effective research practices.

📌 Ocugen Clinical Research Associate Position (Winnipeg)
🏢 OCUGEN OPCO
📍 Winnipeg