Advance your career at PSI as a Senior Clinical Research Associate. This role involves varied monitoring tasks across different therapeutic areas, ensuring your impact on clinical quality is significant.
As part of your responsibilities at PSI, you will conduct monitoring visits, perform essential document reviews, and manage site communications effectively. You'll coordinate with internal teams, contributing to the overall success of clinical studies within a dynamic environment. Your role will be instrumental in upholding our reputation for quality service.
Key Responsibilities:
• Lead monitoring visits including SIV and RMV
• Review CRFs, and conduct source document verification
• Ensure site communication and project management
• Collaborate with internal teams on study progress
• Assist regulatory compliance and document preparation
Requirements:
• Completion of Life Sciences degree or equivalent
• Significant experience in Phase II and/or III monitor...