Take the lead as a Clinical Research Associate with PSI, managing global project timelines and ensuring compliance for clinical trials. Focus on Oncology and advanced therapies.

In this role, you will coordinate site feasibility and monitor patient enrollment for clinical trials. You should have a minimum of four years of site monitoring experience, specifically managing projects in the US. Your strong communication, collaboration, and problem-solving skills will be essential in overseeing diverse project teams and ensuring adherence to regulatory standards across various therapeutic areas, including Oncology.

Key Responsibilities:
• Oversee compliance and manage timelines for clinical trials
• Train and mentor new monitors in the project team
• Facilitate query resolution and monitor essential study documents
• Manage project teams during site contracting and payments
• Conduct audits and prepare training materials for investigat...