Clinical Research Associate – Monitoring Specialist
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In this position, you will ensure the integrity of clinical trials by conducting comprehensive site assessments, verifying consent processes, and maintaining compliance with applicable regulations. You will be tasked with managing site-level activities, communicating effectively with investigators, and contributing to audit readiness. Your expertise in monitoring processes will play a critical role in the success of clinical projects.
Key Responsibilities:
• Conduct on-site and remote monitoring visits
• Verify accuracy of clinical data and site documentation
• Manage inventory and compliance of investigational products
• Document and communicate site performance issues
• Participate in training and meeting preparations
Requirements:
• Experience in site monitoring and clinical research
• Knowledge of GCP and regulatory compliance
• Strong organizational and communication skills
• Ability to adapt to evolving project demands
• Mentorship experience is a plus
Make a significant contribution to advancing clinical trials and ensuring quality in research activities.
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