Having professionals specialized in the field of Clinical Trial Monitoring is essential to achieve positive results’’

The postgraduate certificate in Clinical Trials Monitoring for Nursing offers professionals in this field a global vision of the monitoring process, so that the nurse can learn specialized knowledge that will serve as a guide for the performance of this work in a specialized center. 

Specifically, this program will analyze the design of the protocol, from which the entire clinical trial is developed, and will assess the responsibility of the sponsor to verify the adequate and effective monitoring of the clinical trial. 

Another of the strengths of this program is the development of Monitoring, establishing the most common protocol deviations and specifying solutions for specific cases. 

Relevant aspects such as the monitoring visit and the closing visit, essential documents and source documents, or how to work, in daily practice, with the use of data collection notebooks, among other aspects, will, analyzed. 

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. 

Expand your knowledge through this postgraduate certificate that will allow you to specialize until you achieve excellence in this field’’

This postgraduate certificate in Clinical Trials Monitoring 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 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 Trials
• Practical exercises where the self-assessment process can be carried out to improve learning
• Special emphasis on innovative methodologies in Clinical 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 certificate is the best investment you can make when selecting a refresher program, for two reasons: in addition to updating your knowledge in Clinical Trials Monitoring, you will obtain a qualification endorsed by 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. 

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. 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 Trials  

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

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

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

Thanks to this postgraduate certificate you will be able to specialize in Clinical Trials and learn about the latest advances in the field’’

General objectives

• 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 CE and what is involved at each stage of the clinical trial
• Explain the practical aspects of conducting a CE and the role of the clinical trial monitorSpecific Objectives

Specific objectives

• 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 the correct compliance with the procedures and activities established by the protocol and the standards of good clinical practice during the trial
• 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
• Establish the basic points of a monitoring and closing visit
• Develop the monitor's 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

A unique specialization program that will allow you to acquire advanced training in this field"