Join Ocugen as a Clinical Research Associate to oversee critical clinical trials. Ensure compliance and participant safety while gaining invaluable hands-on experience.
This dynamic position involves supporting the planning, management, and closeout of Phase 1-3 trials. You'll coordinate essential activities at investigational sites, provide operational support, and monitor data integrity in line with ICH GCP standards. Quality and participant safety are at the forefront of your responsibilities.
Key Responsibilities:
• Manage start-up and closeout operations for clinical studies
• Facilitate documentation and site feasibility activities
• Serve as a key link for data entry and issue resolution




• Track study metrics and provide risk assessments
• Coordinate investigational product logistics and documentation
Requirements:
• Bachelor’s degree in relevant life sciences
• At least three years in a clinical research role
• Expertise in GCP and relevant regulations
• Familiarity with clinical trial management systems
• Solid interpersonal and communication skills
Capitalize on your clinical research experience at Ocugen and improve patient safety through cutting-edge studies.
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📌 Ocugen Clinical Research Associate Position (Toronto)
🏢 Ocugen
📍 Toronto