Become a key player as a Senior Clinical Research Associate, where site management and compliance are your top priorities. This role encompasses both remote and on-site monitoring tasks.

As part of our clinical monitoring team, you will oversee site qualification, monitor compliance with protocols, and assess patient safety. Your critical thinking and problem-solving skills will facilitate communication regarding site performance and support compliance with ICH/GCP guidelines. You'll be involved in mentoring junior CRAs and ensuring project timelines are met.

Key Responsibilities:
• Monitor site operations and compliance standards
• Prepare for and document investigator meetings
• Conduct audits and prepare for sponsor visits
• Perform data verification and query resolution
• Support patient recruitment and retention efforts

Requirements:
• Bachelor's degree or equivalent experience
• Comprehensive knowled...