Join the interdisciplinary team at WELL Health Diagnostic Centres as a Clinical Research Coordinator. Shape the future of healthcare by managing clinical trial activities and supporting patient enrollment.
In this role, you will oversee daily operations of clinical trials, ensuring compliance with regulatory guidelines and facilitating smooth workflow among team members. Your responsibilities include participant recruitment, data management, financial tracking, and monitoring regulatory compliance. Drive impactful research that contributes to better health outcomes.
Key Responsibilities:
• Coordinate the day‑to‑day activities of clinical trials
• Liaise with internal departments for research approval processes
• Report and manage adverse events per protocol requirements
• Prepare for monitoring visits and audits as needed
• Develop study budgets and manage financial responsibilities
Requirements:
• Minimum of 3 years of relevant clinical research experience