Research Analyst

• Provide strategic oversight and management of clinical trial sites
• Ensure protocol compliance, data integrity, and the protection of patient safety and rights
• Drive study quality and performance through risk-based monitoring and proactive risk management
• Collaborate with site staff and cross-functional teams to ensure the successful execution of trials
• Act as a Site Manager and build trusted partnerships with investigators and site staff
• Conduct on-site and remote visits in accordance with the Monitoring Plan, Protocol, ICH-GCP, internal SOPs and regulatory requirements
• Drive the implementation of Risk-Based Quality Management (RBQM) principles
• Oversee site performance, recruitment progress, retention and data collection
• Manage IMP, study supplies, essential documents and the Investigator Trial Master File

Clinical Research Associate 2

• Delivering clinical trial monitoring work to a high standard
• Working independently and actively to coordinate all activities for setting up and monitoring a study
• Completing accurate study status reports and maintaining study documentation
• Running sponsor generated queries efficiently and taking responsibility for study cost efficiency
• Participating in the preparation and review of study documentation and feasibility studies for new proposals as required
• Developing and maintaining strong, collaborative relationships with key stakeholders, clinical investigators, and site staff
• Ensuring patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements

Clinical Research Associate

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
• Conducting site visits to assess site performance, resolve issues, and provide support
• Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting
• Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct
• Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations

Research Analyst jobs in Italy

See all jobs on JobTailor

Clinical Research Associate 2

Clinical Research Associate

Senior Clinical Research Associate