Analytical Monitor

Tasks

• Address deviations from protocol
• Collaborate with clinical sites
• Collaborate with external vendors
• Collaborate with study teams
• Collect clinical trial data
• Coordinate central review logistics
• Coordinate central review scheduling
• Coordinate imaging assessments
• Coordinate laboratory analyses
• Ensure adherence to protocol requirements
• Ensure adherence to regulatory standards
• Execute central review activities
• Identify issues in central review process
• Interpret clinical trial data
• Maintain central review documentation
• Maintain centralized evaluation records
• Monitor central review progress
• Monitor central review quality
• Provide stakeholder guidance on best practices
• Provide stakeholder guidance on central review methodologies
• Provide stakeholder guidance on protocols
• Transfer clinical trial data

Perks/Benefits

• Dental insurance
• Disability coverage
• Employee assistance program
• Health insurance
• Learning and development
• Life assurance
• Pension plan
• Retirement plan
• Vision insurance
• Wellbeing resources

Skills/Tech-stack

Clinical Research | Clinical trials | Cross-Functional Collaboration | Cross-functional | Data Integrity | Data Management | Data Quality | Documentation | Functional collaboration | Imaging Assessment | Laboratory analysis | Logistics | Problem Solving | Project Management | Protocol compliance | Quality management | Regulatory Compliance | Scheduling | Stakeholder management