RBM Site Monitoring Lead

Job Summary

To enhance clinical trial management, the full-time salaried RBM Site Monitoring Lead will oversee site monitoring activities, ensuring compliance and quality while working remotely.

Key responsibilities

• Manage site monitoring plans and ensure adherence to regulatory requirements
• Collaborate with cross-functional teams to optimize site performance and patient recruitment
• Conduct risk assessments and implement strategies to mitigate potential issues at trial sites

Required qualifications

• Bachelor's degree in a relevant field or equivalent experience
• Proven experience in site monitoring or clinical trial management
• Strong understanding of GCP, ICH guidelines, and regulatory requirements
• Experience with risk-based monitoring approaches
• Ability to work independently and manage multiple projects simultaneously