Thank you for participating in the Alina study
We are grateful for your participation in this study.
This website is designed to provide you with some helpful resources as you navigate through the ALINA study.
Watch our patient video
Newsletter
Newsletter
Helpful Resources
For these and other helpful resources, please visit younity.global.
Study team
Roles & Responsibilities
Roles and responsibilities might vary per country or region.
Principal Investigator
The principal investigator supervises all aspect of the clinical trial. Everything from the recruitment of patients to the informed consent process, as well as data collection, analysis, interpretation and presentation, is the responsibility of the principal investigator.
Study Coordinator
The study coordinator is responsible for helping to coordinate the study, including administrative responsibilities on behalf of the principal investigator. In addition, they act as a liaison between the study site and study sponsor as well as review all data and records to ensure quality and consistency.
Research Nurse
The research nurse supports the study through multiple aspects. This includes educating staff, communicating with patients, and informing health care providers about the trial. Additionally, the research nurse will support the principal investigator with the informed consent process, study monitoring, quality assurance, data management and analysis.
Site Physician/Nurse
These health care professionals aid in taking care of the study participants throughout the clinical trial. This would include treating participants in accordance with the clinical trial protocol, assess and record how each participant responds to the treatment and manage the care of study participants. They collaborate with the principal coordinator and research nurse to follow the health of study participants.
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