Pharmacists who wish to develop their work in the field of Clinical Trial Coordination will find in this postgraduate diploma the most complete and up to date education on the market"

The coordinator of a clinical trial must have extensive knowledge of the unit to be investigated, the sector, related products, etc. In addition, they must have a clear understanding of the regulations in force on the subject, in order to avoid any hindrance that could lead to a setback in the research. Likewise, you must keep absolute control over all the steps to be followed in each process, so it is essential that you record all the information related to the investigation.

For this purpose, this person must have a file that gathers all the documentation related to the research team (Curriculum Vitae and other relevant documents that evidence the qualification of the researchers) and to the patient (informed consents, recruitment measures, monitoring visits), the study protocol, the researcher’s manual, a model of the data collection notebook, and the different laboratory and safety procedures, so its safekeeping must be carried out in an adequate manner.

In order to know the best way to carry out the coordination work, this postgraduate diploma has compiled all the information related to the clinical trial and 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 education has a specialized program 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 pharmacists. 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 combine it perfectly with the rest of your daily obligations.

This postgraduate diploma will allow you to specialize in Clinical Trials Monitoring until you achieve excellence in your work"

This postgraduate diploma in Clinical Trial Coordination contains the most complete and up-to-date educational 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 development
• 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 university experts, 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 an up-to-date program for two reasons: in addition to updating your knowledge in Clinical Trial Coordination, you will obtain a degree endorsed by the TECH Global University"

The teaching staff includes professionals from the Health sector, who bring their experience to this training 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 training programmed to train 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 Trials Coordination

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

This 100% online 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 Coordination is aimed to facilitate the activities 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

• Train the student in the handling and management of the 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 specialty 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, etc.
• 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, biological) 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

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