Clinical Data Analyst

As Clinical Risk Management functional lead, the Clinical Data Analyst is responsible for set-up and implementation of Central Monitoring

• Recognize, exemplify and adhere to ICON's values which center around our commitment to People, Clients and Performance.
• As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
• Provide input to study risk assessment and propose appropriate and tailored risk indicators for central analysis, in line with holistic data monitoring model
• Create and own the Central Monitoring Plan
• Support set-up and testing of data analysis platform
• Review clinical study data and make independent decisions to identify potential site performance and site organization issues
• Train and support the project teams about interpretation of Central Monitoring outputs and relevant decision making for study conduct
• Manage operational risk log for Clinical Risk Management activities
• Support preparation, conduct and follow-up of the Quality Risk Review Meetings for effective communication with the cross functional project team to ensure adequate decisions are taken about the study monitoring strategy and effective resolution of site performance issues
• Oversee Clinical Risk Management project budget, scope of work, forecasting* Support cross-functional and external ICONik users with system use.
• Act as mentor for Central Monitoring team members.
• Support internal and external promotion of Central Monitoring and related systems.
• Travel (approximately 5%) domestic and/or international.
• Other duties as assigned

• Provide input to study risk assessment and propose appropriate and tailored risk indicators for central analysis, in line with holistic data monitoring model
• Create and own the Central Monitoring Plan
• Support set-up and testing of data analysis platform
• Review clinical study data to identify potential site performance and site organization issues
• Train and support the project teams about interpretation of Central Monitoring outputs and relevant decision making for study conduct
• Manage operational risk log for Clinical Risk Management activities
• Communicate effectively with the project team, CRAs, Project Managers, Clinical Trial Managers, DM Staff, Medical staff, Scientific Council to ensure adequate decisions are taken about the study monitoring strategy and effective resolution of site performance issue
• Oversee Clinical Risk Management project budget, scope of work, forecasting