Swiss Medical GroupClinical Research Coordinator
May. 2022 - May. 2023• Provide technical and administrative support to the principal investigator.
• Collect and maintain investigation and site documents (Master Files).
• Preparation of monitoring activities, audits, and inspections; electronic upload of study data; response to inquiries; training and adherence to the protocol, ICH-GCP, and local regulations.
• Start-up tasks: preparing all the necessary documentation for the study.
• Constantly communicate with regulatory agencies, ethics committees, suppliers, and CRO.