See further information on possible conflicts of roles and objectives of healthcare staff when collecting treatment data for later use for research purposes:

Central Ethics Committee at the German Medical Association (2023). Provision and use of treatment data for research purposes. Deutsches Ärzteblatt, 120(9), A-409 / B-349, 7-12. https://doi.org/10.3238/arztebl.zeko_sn_behandlungsdaten2022_en

Beauchamp, T. L., & Childress, J. F. (2019) Principles of Bioethics (8th edition). Oxford University Press, Chapter 8, Section Privacy. 

Richards, M., Anderson, R., Hinde, S., Kaye, J., Lucassen, A., Matthews, P. M., Parker, M., Shotter, M. V., Walls, G., Wallace, S. E., & Wise, J. (2015). Chapter 2 - Data opportunities and threats. In  Nuffield Council on Bioethics, (Ed.), The collection, linking and use of data in biomedical research and health care: ethical issues (pp. 22-44). https://cdn.nuffieldbioethics.org/wp-content/uploads/Biological_and_health_data-report.pdf

Jungkunz, M., Kongeter, A., Winkler, E. C., & Schickhardt, C. (2024). Do Physicians Have a Duty to Support Secondary Use of Clinical Data in Biomedical Research? An Inquiry into the Professional Ethics of Physicians. Journal of Law, Medicine & Ethics, 52(1), 101-117. https://doi.org/10.1017/jme.2023.146