Join Ocugen as a Clinical Research Associate to oversee critical clinical trials. Ensure compliance and participant safety while gaining invaluable hands-on experience.This energetic 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 studiesFacilitate documentation and site feasibility activitiesServe as a key link for data entry and issue resolutionTrack study metrics and provide risk assessmentsCoordinate investigational product logistics and documentationRequirements:Bachelor's degree in relevant life sciencesAt least three years in a clinical research roleExpertise in GCP and relevant regulationsFamiliarity with clinical trial management systemsStrong interpersonal and communication skillsCapitalize on your clinical research experience at Ocugen and improve patient safety through cutting-edge studies.

📌 Ocugen Clinical Research Associate Position (Toronto)
🏢 Ocugen
📍 Toronto