Shape the future of clinical trials with Ocugen as a Clinical Research Associate. Oversee Phase 1-3 studies while ensuring participant safety and data integrity in a dynamic environment.

This Canada-based position is integral to the clinical research team, handling the planning, start-up, execution, oversight, and closeout of clinical studies. As a Clinical Research Associate, you will coordinate site activities, maintain essential documentation, and collaborate with CROs to ensure compliance with ICH Valuable Clinical Practice standards. A strong background in clinical research and relevant education is essential for success.

Key Responsibilities: • Support start-up, execution, and closeout of clinical trials • Coordinate site identification, qualification,



and training • Oversee monitoring and quality assurance activities • Maintain accurate study trackers and documentation • Manage investigational product tracking and related activities

Requirements: • Bachelor’s degree in life sciences, nursing, or pharmacy • At least three years of clinical research experience • Familiarity with eTMF, CTMS, and EDC systems • Knowledge of ICH GCP and regulatory requirements • Strong organizational and problem-solving abilities

Drive excellence in clinical study management through meticulous oversight and collaboration at Ocugen. #J-18808-Ljbffr

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