69.00€
In the “Introduction to Trial Master File” course, you will learn everything you need to know to get started with the most important and essential tool used in all clinical trials. There isn’t a person in clinical research who hasn’t encountered the need to work with TMF, so all the information you’ll learn at the end of the course will get you started safely or will structure the information you already have.
Not sure what TMF is and what it’s used for? Not sure how to get your team to work together or what to use?
After completing this course, you’ll learn what is involved in working with clinical documentation, what tools are available to you, and why it’s so important. You will learn the very preliminary regulations that guide TMF work and how to encourage your teammates to do this activity.
Are you terrified at the very thought of a TMF inspection in your study? This course will show you how to take action to keep the stress of the inspection to a minimum while still succeeding at it.
Are you planning to start working with TMF or have just started, but don’t quite understand its complexities? 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.
Don’t miss out on this opportunity to revolutionize your employee development process with AIDIFY’s freemium license. Fill out our form to get started today!
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