Discover what's new in Clinical Trial Monitoring and give your career a boost. This program will help you grow professionally and personally"

Pharmacology research is a fundamental task in the search for treatments to improve the health of patients. Moreover, it is a booming sector, as more and more public and private institutions have realized the need to invest in research, allocating more resources to this cause. And, therefore, there is also a new need for better prepared and qualified professionals to carry out the tasks of monitoring these investigations. 

To this end, this postgraduate diploma offers a complete education in this field, in which the students will be able to discover from the design of the protocol from which the entire clinical trial is developed, and assess their responsibility for the verification of the adequate and effective monitoring of the clinical trial, to the close relationship that exists between the trial promoter and the monitor. 

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 allow you to specialize in Clinical Trial Monitoring until you achieve excellence in your work"

This postgraduate diploma in Clinical Trial Monitoring 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 Trial Monitoring
• 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 on Clinical Trials Monitoring
• Practical exercises where self-assessment can be used to improve learning
• Special emphasis on innovative methodologies in Clinical Trial Monitoring
• 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, you will obtain a diploma endorsed by the TECH Global University”

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.

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. To do so, the professional will be assisted by an innovative interactive video system created by renowned and experienced experts in the field of Clinical Trial Monitoring. 

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

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

The postgraduate diploma in Clinical Trial Monitoring 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 specialize in Clinical Trial Monitoring and learn about 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 investigator's 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)

Module 2. Monitoring of Clinical Trials (I)

• Disclose the types of fraud committed in clinical trials research
• 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 (SOPs) 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 Events (AEs) and Serious Adverse Events (SAEs)
• 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

Make the most of this opportunity to learn about the latest advances in this subject to apply it to your daily practice"