Php help cra javascript jquery állások XXIII. kerületben (klinikai kutató)

• Performing and coordinating different aspects of the clinical monitoring and site management process
• Conducting remote or on-site visits to assess protocol and regulatory compliance and managing required documentation

• Performing and coordinating different aspects of the clinical monitoring and site management process
• Conducting remote or on-site visits to assess protocol and regulatory compliance and managing required documentation

• Coordinating, overseeing and completing functions on assigned trial(s) activities as detailed on the task matrix according to the specific role (Central or Local)
• Performing department, Internal, Country and Investigator file reviews as assigned, and documenting findings in appropriate system(s)

Preparing, reviewing and coordinating, under guidance, local regulatory submissions (MoH, EC, additional special national local applications if applicable, e.g. gene therapy approvals, viral safety dossiers, import license) in alignment with global submission strategy...

• Providing medical leadership to the study teams, including creating clinical trial protocols while implementing the latest scientific information
• Contributing to site selection

Monitoring investigator sites with a risk-based monitoring approach applying root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks...

• Providing medical leadership to the study teams, including creating clinical trial protocols while implementing the latest scientific information
• Contributing to site selection