Proper coordination of investigations is essential to achieve effective and quality results. Don't miss the opportunity to learn with us"

The figure of the coordinator is essential in any type of research to ensure that all the work is carried out properly and in accordance with current regulations. In addition, they are responsible for recording all the information related to the research, taking into account that the investigator's file should contain all the documentation related to the research team (curriculum vitae and other relevant documents that evidence the qualification of the researchers) and the patient (informed consents, recruitment measures, monitoring visits), the study protocol, the investigator's manual, a model of the data collection notebook, and the different laboratory and safety procedures, and should therefore be kept in an adequate manner. 

In this sense, this postgraduate diploma analyzes the importance of the investigator's file, as well as the figure of the Clinical Trial Coordinator and their main responsibilities, the vital importance of the trial process and everything that surrounds it. 

This program has a syllabus of the highest academic level that has been designed by a team of specialists with years of professional and teaching experience. A multidisciplinary program that aims to broaden the knowledge of nurses. And all of this with a 100% online format thanks to which you will be able to self-manage your study time, deciding where and when to study. No time limits or need to move to a physical space, so you can balance it perfectly with the rest of your daily obligations.

This postgraduate diploma in Clinical Trials Coordination for Nursing will enable you to achieve excellence in your profession"

This postgraduate diploma in Clinical Trials Coordination for Nursing contains the most complete and up-to-date scientific program on the market. The most important features include:

• The development of case studies presented by experts in Clinical Coordination of Trials
• The graphic, schematic, and practical contents with which they are created, provide scientific and practical information on the disciplines that are essential for professional practice
• New developments in Clinical Coordination of Trials
• Practical exercises where the self-assessment process can be carried out to improve learning
• Special emphasis on innovative methodologies in Clinical Coordination of Trials
• Theoretical lessons, questions to the expert, debate forums on controversial topics, and individual reflection work
• Content that is accessible from any fixed or portable device with an internet connection

This postgraduate diploma is the best investment you can make in the selection of a refresher program for two reasons: in addition to updating your knowledge in Clinical Trial Coordination, you will obtain a postgraduate diploma from TECH"

The teaching staff includes professionals from the Health field, who bring their experience to this educational program, as well as renowned specialists from leading societies and prestigious universities. 

The multimedia content, developed with the latest educational technology, will provide the professional with situated and contextual learning, i.e., a simulated environment that will provide immersive education programmed to learn in real situations. 

This program is designed around Problem-Based Learning, whereby the professional must try to solve the different professional practice situations that arise throughout the program. For this purpose, the professional will be assisted by an innovative interactive video system developed by renowned and experienced experts in the field of Clinical Trial Coordination.

This 100% online postgraduate diploma will allow you to combine your studies with your professional work while expanding your knowledge in this field"

Do not hesitate to take this educational program with us. You will find the best teaching material with virtual lessons"

The postgraduate diploma in Clinical Trials Coordination for Nursing is aimed at facilitating the performance of the research professional with the latest advances in the sector.   

Thanks to this postgraduate diploma you will be able to you to learn about Clinical Trials Coordination and delve into the latest advances in the field”

General Objectives

• Prepare the student in the handling and management of researcher's archive documentation in accordance with current regulations, the GCP and ICH
• Develop legislative knowledge governing the documentation of the investigator's file
• Analyze the importance of the role of the trial coordinator in clinical research
• Specify the main functions of the research team and their involvement with the patient
• Establish the main components of a clinical trial and observational study
• Examine the treatment of patients within the context of a clinical trial, both in the Specialized Care and in hospitalization
• Develop specialized knowledge about the variety of tasks they have to perform during the development of the study
• Establish tools and strategies to approach the different problems that arise during the clinical trial, in order to obtain satisfactory results in patient monitoring

Specific Objectives

Module 1. Coordination of Clinical Trials I

• Specify the mandatory documents and forms that must be included in the researcher’s file
• Establish how to best manage the archive at the beginning, during and at the end of the study: storing, updating and ordering documentation
• Define the steps to be followed to complete the documents and forms for the researchers file

Module 2. Coordination of Clinical Trials II

• Substantiate the necessary skills to be developed in order to perform the work of the trial coordinator
• Define the organization and preparation of both the research team and the center, for inclusion in a clinical trial, managing the CV, good clinical practices, suitability of the facilities, among others
• Reproduce the tasks to be performed in both a clinical trial and an observational study
• Analyze a clinical trial protocol through theoretical and practical examples
• Determine the work of a Coordinator in their work center under a clinical trial protocol (patients, visits, tests)
• Develop the skills necessary for the use of a data collection notebook: data entry, query resolution and sample processing
• Compile the different types of pharmacological treatments that can be used in a clinical trial (placebo, biologic) and their management

Module 3. Follow-up of Patients in Clinical Trials

• Specify the daily practices of patient care in Specialized Care, establishing the management of procedures, protocols and databases of clinical trials
• Analyze the materials used during the development of the studies
• Assess the causes of patient dropout within a study and establish strategies for patient retention
• Assess how monitoring loss occurs in patients within a study, examine its causes and explore possibilities for resumption of monitoring
• Compile the different risk factors that can lead to poor adherence to treatment, and apply strategies for improving and monitoring adherence to treatment
• Analyze the different presentations of medications in order to manage the signs and symptoms, as well as the adverse reactions that may derive from taking medication
• Establish the different tools to calculate the attendance and monitoring of visits

An intensive course that will allow you to become a postgraduate diploma in Clinical Trials Coordination for Nursing in a short period of time and with the greatest flexibility"