Selecting Clinical Trial Sites

Learning Elements provides an understanding of the patient information and informed consent process understand how to verify that the process of obtaining informed consent has been adequately performed and documented…

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Initiating Clinical Trial Sites

Learning Elements provides an understanding of the patient information and informed consent process understand how to verify that the process of obtaining informed consent has been adequately performed and documented…

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Monitoring Clinical Trial Sites

Learning Elements provides an understanding of the patient information and informed consent process understand how to verify that the process of obtaining informed consent has been adequately performed and documented…

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Closing Clinical Trial Sites

Learning Elements provides an understanding of the patient information and informed consent process understand how to verify that the process of obtaining informed consent has been adequately performed and documented…

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Oncology Study Design

Learning Elements provides an understanding of the patient information and informed consent process understand how to verify that the process of obtaining informed consent has been adequately performed and documented…

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The Role of the Clinical Trial Assistant

Learning Elements provides an understanding of the patient information and informed consent process understand how to verify that the process of obtaining informed consent has been adequately performed and documented…

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Clinical Research Stakeholder Management

Learning Elements provides an understanding of the patient information and informed consent process understand how to verify that the process of obtaining informed consent has been adequately performed and documented…

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Introduction to Study Start Up

Learning Elements provides an understanding of the patient information and informed consent process understand how to verify that the process of obtaining informed consent has been adequately performed and documented…

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Clinical Research Project Management Basics

Learning Elements provides an understanding of the patient information and informed consent process understand how to verify that the process of obtaining informed consent has been adequately performed and documented…

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Clinical Research Data Management Basics

Learning Elements provides an understanding of the patient information and informed consent process understand how to verify that the process of obtaining informed consent has been adequately performed and documented…

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From Medicines Development to Clinical Research

Learning Elements Background of medicines development Research and discovery stage & product development Clinical development Regulatory submission, Health Technology Assessment, lifecycle management ICH GCP and other applicable regulations Learning Outcomes…

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Regulatory Environment in the EU and USA

Learning Elements applicable national and international regulatory requirements including ICH GCP E6 (R2) requirements for audits and inspections need of compliance in all activities of your future professional work sponsor’s…

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The Investigational Medicinal Product Management

Learning Elements provides an understanding of what an investigational product (IP) is (including comparators and placebo) provides an understanding of how the defined investigational drug(s) need to be managed (e.g.…

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Patient Protection and the Informed Consent

Learning Elements provides an understanding of the patient information and informed consent process understand how to verify that the process of obtaining informed consent has been adequately performed and documented…

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Clinical Monitoring Adverse Events

Learning Elements enables learners to identify adverse events and to differentiate between the types of adverse events according to the ICH guidelines and to take the required reporting actions familiarizes…

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Clinical Research Fundamentals

Start your career in clinical research with our Clinical Research STARTER Program. You will acquire basic knowledge about clinical research and learn from and with industry experts. In this program,…

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VIARES Clinical Research Associate

Our Clinical Research Academy is a great way to join the clinical research industry. This program is designed for great talents who are eager to start the clinical research career…

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VIARES Study Start Up Specialist

The VIARES Study Start Up Specialist program is more than just training. We aim to improve employability as Clinical Research Professionals for our participants. Our setup enables participants to complete…

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VIARES Clinical Research Data Management

The VIARES Clinical Research Data Management program is more than just training. We aim to improve employability as Clinical Research Professionals for our participants. Our setup enables participants to complete…

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VIARES ACADEMY MARCH 2020

Our Clinical Research Academy is a great way to join the clinical research industry. This program is designed for great talents who are eager to start the clinical research career…

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CTA Academy Self Paced

Start your career in clinical research as a clinical trial assistant! With our online CTA Academy, produced by veteran trainers you’ll understand the big picture of medicine development, the roles…

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