69.00€
The Good Clinical Practice recommendations treat not only the management of clinical trials from the sponsor’s perspective but also, to a large extent, address the subject of the Investigator.
It is this topic that we address in the Good Clinical Practice from Investigator`s perspective course.
Do you work on the side of a clinical trial site and would like to learn a little more about the practical implementation of Good Clinical Practice principles? Are you an investigator, co-investigator, coordinator, nurse, or Data Entry on the site side and want to make sure you can implement GCP theories in practice?
Or are you a CRA and would like to better understand what an investigator and a team face during the day-to-day work of conducting clinical trials according to GCP?
Or do you simply want to expand your knowledge in the area of understanding and implementation of GCP?
If the subject of GCP implementation at the site is something you would like to explore, then this course is for you!
She has been involved in the clinical research industry since 2015. She currently works for a global pharmaceutical company as a Manager in the Clinical Documentation team, where her main role is FSO Operations Lead.
She places high value on personal development and the quality of performed activities, which makes her a valued member of project teams. She has operational experience gained in global CROs and pharmaceutical companies. She has worked on both investigational and medical device projects in a variety of therapeutic areas.
From the very beginning of her work in clinical research, she has struggled with the complex nature of clinical trial documentation and TMF, which she continues to explore to this day.
In addition to her day job, she is actively involved in the academic community, initially as a coordinator and support to the manager of a post-graduate study in the clinical trial area. Currently, she is a lecturer at Conducting and Monitoring Clinical Trials and a manager of postgraduate study Project Management in Clinical Trials.
This collaboration started after the previously completed postgraduate studies in Conducting and Monitoring Clinical Trials. Graduate of Nicolaus Copernicus University in Torun in the faculties of molecular biology and environmental protection.
Although she started her professional life at the Central Forensic Laboratory of the Police, she now finds herself perfectly at work in clinical project activities and now she is conducting other types of investigations.
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