Join PSI as a Senior Clinical Research Associate, specializing in site management and patient enrollment within Oncology. Your leadership will drive project success and compliance.

As a Senior Clinical Research Associate at PSI, you will lead site monitoring and manage the operational oversight of clinical studies. This role requires a minimum of four years of monitoring experience in the US, ensuring compliance with regulatory guidelines while coordinating project timelines and feasibility assessments. You'll thrive in a challenging environment where you will use your strong communication skills and advanced knowledge of clinical trials.

Key Responsibilities:
• Manage project timelines and properly oversee patient recruitment
• Coordinate safety information flow and monitor deviations
• Conduct site audits and prepare for investigator meetings
• Deliver ongoing training for monitoring team members
• Supervise contract and payment...