Take charge of clinical studies at PHRI as a Research Project Coordinator II. This role involves coordinating meetings, managing data, and overseeing essential documents for successful study execution.
As a Research Project Coordinator II, you will support clinical studies through effective coordination and management. Key tasks include planning study meetings, tracking site usage, and assisting with regulatory applications. Your analytical skills will help ensure productive data management and monitor ongoing site activities.
Key Responsibilities:
• Plan and organize study meetings and teleconferences
• Track IP usage and create projection reports
• Design and manage outcome event adjudication materials




• Coordinate site start-up processes and documentation
• Oversee data management and reporting procedures
Requirements:
• Undergraduate degree in Biology or Health Sciences
• Minimum 2 years in multi-centre research studies
• Experience with managing large clinical datasets
• Knowledge of ICH-GCP Guidelines and regulations
• Proficient in Microsoft Office and data capture systems
Leverage your communication and analytical skills to enhance clinical studies at PHRI while ensuring adherence to research methodologies.
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📌 Clinical Study Coordinator at PHRI (Hamilton)
🏢 Socket.dev
📍 Hamilton