Investing in research is important, but so is having specialized professionals" For this reason, at TECH we have designed this very complete program"

Clinical research is essential in order to find new drugs to control and cure newly emerging diseases that do not have a cure or are increasingly resistant to existing drugs. Therefore, it is essential to continue preparing in this field, which will allow nurses to specialize in Clinical Trial Monitoring for Nursing.

Clinical Trial Monitoring is one of the fundamental aspects of research. This postgraduate diploma defines the figure of the promoter, an essential element for the design and conduct of research. To this end, the main functions of the sponsor are analyzed, including the design of the protocol on the basis of which the entire clinical trial is developed, and the sponsor's responsibility is assessed in relation to the verification of the adequate and effective monitoring of the clinical trial, thereby establishing the close relationship between the sponsor and the monitor. 

In this way, it specifies the profile of the monitor and the skills and abilities to ensure the proper functioning of the study within the research center, complying with the Good Clinical Practice standards and the requirements of the protocol. 

In short, a global vision of the monitoring process is presented, so that the healthcare professional will be able to acquire specialized knowledge that will serve as a guide for carrying out this work in a specialized center. In addition, as it is a 100% online postgraduate diploma, the students are the ones who decide where and when to study, for which they only need a computer or mobile device with internet connection.

This postgraduate diploma will enable you to learn about Clinical Trial Monitoring for Nurses until you achieve excellence in your work"

This postgraduate diploma in Clinical Trials Monitoring for Nursing contains the most complete and up-to-date scientific program on the market. Its most notable features are: 

• The development of case studies presented by experts in Clinical Trial Monitoring. for Nursing
• 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
• What's New in Clinical Trial Monitoring for Nurses?
• Practical exercises where self-assessment can be used to improve learning
• Its special emphasis on innovative methodologies in Clinical Trial Monitoring for Nursing
• Theoretical lessons, questions to the expert, debate forums on controversial topics, and individual reflection assignments
• 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 Monitoring for Nursing, you will obtain a qualification endorsed by TECH"

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

Its multimedia content, developed with the latest educational technology, will allow the professional a situated and contextual learning, that is, a simulated environment that will provide an immersive learning programmed to prepare for real situations.

The design of this program focuses on problem-based learning, by means of which the healthcare professional must try to solve the different professional practice situations that arise throughout the academic program. To do so, the professional will be assisted by an innovative interactive video system developed by recognized experts in the field of Clinical Trial Monitoring for Nurses with extensive experience.  

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

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

The postgraduate diploma in Clinical Trial Monitoring 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 learn about Clinical Trial Monitoring for Nursing and delve into the latest advances in the field"

General Objectives

• Establish the basic structure of a Clinical Trial
• Justify the difference between different types of clinical trials
• Compile the essential documents and procedures within a clinical trial
• Establish the different roles that exist in the figure of the clinical trial sponsor, their function and their relationship with the research center
• Substantiate the concept of monitoring
• Analyze the content of a clinical research protocol and recognize the commitment that a good compliance with it entails
• Master the skills necessary for project development and management
• Define the process of monitoring a clinical trial, with the necessary documentation, tools and guidance for this role, taking into account the main problems that may be encountered
• Present the latest scientific advances in clinical trial monitoring tasks, with knowledge adapted to the real needs of companies in the pharmaceutical sector
• Present the wide range of tasks involved in conducting a CT and what is involved at each stage of the clinical trial
• Substantiate the practical aspects of conducting a CE and the role of the clinical trial monitor

Specific Objectives 

Module 1. Clinical Trials I

• Establish the types of clinical trials and standards of good clinical practice
• Specify the processes of authorization and distinction of drugs and medical devices in research
• Analyze the evolutionary process of drug research development
• Specify strategies for developing a safety surveillance plan for marketed drugs
• Substantiate the necessary requirements for the initiation of research with drugs in humans
• Establish the elements of a clinical trial research protocol
• Substantiate the difference between inferiority and non-inferiority clinical trials
• Compile the essential documents and procedures within a clinical trial
• Specify the utility and learn the use of data collection notebooks (DCNs)
• Analyze the variety of avenues for the development and funding of non-commercial research
• Disclose the types of fraud committed in clinical trials research

Module 2. Monitoring of Clinical Trials I

• Specify both the professional profile of the clinical trial monitor and the skills that must be developed to carry out the monitoring process of a clinical trial
• Establish your responsibility in the selection of the center and in the initiation of the study
• Justify the importance of the monitor in ensuring, during the trial, the correct compliance with the procedures and activities established by the protocol and the Good Clinical Practice Guidelines
• Generate knowledge on the practical aspects of visits prior to the start of the clinical trial
• Present the basis for the essential documentation for the implementation of the clinical trial at the center
• Prepare the student in the correct handling of a pre-selection visit and initiation in the research center
• Assess the involvement of the Hospital Pharmacy Service in the management, control and traceability of the medication in the study
• Justify the importance of maintaining good communication between team members involved in the development of a clinical trial

Module 3. Monitoring of Clinical Trials II

• Establish the basic points of a monitoring and closing visit
• Develop the Monitoring Plan and Standard Operating Procedures (SOP) at each stage of the clinical trial
• Present a data collection notebook and specify how to keep it up-to-date
• Establish the data collection process to assess safety in a clinical trial. Adverse Event and Serious Adverse Event
• Reproduce the management of a monitoring visit
• Analyze the most common protocol deviations
• Establish the important documents for a clinical trial
• Submit a Clinical Trial monitor’s guideline (Monitoring plan)
• Present the data collection notebooks
• Develop important theoretical knowledge about closeout visits
• Establish the documentation to be prepared for closeout visits
• Specify the points to be reviewed in the closeout visits
  
  

Enter one of the most creative and exciting fields in the world of gastronomy with the background of a complete professional, qualified to successfully lead any project"