Drive innovative clinical research at Ocugen as a Clinical Research Associate. Manage the execution of critical clinical trials while ensuring compliance and data integrity. This exciting role is located in Canada and involves overseeing the start-up, maintenance, and closeout of Phase 1-3 clinical trials.

You will act as a liaison between investigational sites, CROs, and internal teams, ensuring participant safety and data accuracy in adherence to regulatory standards. Your clinical research expertise will be pivotal in driving study success. Key Responsibilities:

- Oversee execution and closeout of clinical trials
- Serve as operational contact for investigational sites
- Coordinate and maintain essential study documentation
- Review performance data and manage risks
- Facilitate training and monitoring for field CRAs Requirements:
- Bachelor’s in life sciences or related discipline
- Minimum three years in a clinical research setting
- Knowledge of ICH E6(R3) GCP and relevant regulations
- Experience with ophthalmology or advanced therapies preferred
- Excellent communication and team-oriented skills Contribute to Ocugen’s commitment to quality and compliance within clinical research operations.

📌 Clinical Trials Associate Role at Ocugen (Toronto)
🏢 OCUGEN OPCO
📍 Toronto