Direct clinical project operations, leading trials from setup to closure. Ensure compliance, manage budgets, and elevate sponsor satisfaction through effective oversight.
In this role, you'll be responsible for the complete management of clinical projects, ensuring adherence to GCP, ICH guidelines, and relevant regulations. You’ll collaborate closely with cross-functional teams to meet project objectives while monitoring risks and performance metrics. Preparing and maintaining essential project documentation is also a key function.
Key Responsibilities:
• Execute comprehensive management of clinical trials
• Ensure compliance with regulatory standards and project guidelines
• Direct cross-functional team coordination and communications
• Manage project timelines, budgets, and performance metrics
• Participate in audits, inspections, and quality improvement
Requirements:
• At least 3 years in clinical project management
• Experience in CRO, pharmaceutical, ...