Learn about the functions of a Principal Investigator, a Monitor and a Sponsor, to adapt your professional profile to the figure that most interests you" 

In a Clinical Trial there are different figures that form a relevant part of the process, in addition to the Principal Investigator. The Sponsor who is in charge of bringing together the specialists who will carry out the study, as well as the Monitor, who is the link between this team and what is usually a development company, stand out. These professions are constantly on the rise and require in-depth and advanced specialization.

For this reason, TECH  has designed a postgraduate certificate in Clinical Trials, Principal Investigator, Monitor and Sponsor, to provide students with the necessary skills and competencies to address these functions with total efficiency and specific knowledge. In this way, the contents delve into topics such as Study Design, Evidence-Based Veterinary Medicine, Ethical and Legal Regulations, the Research Team and Quality Control or Sponsors of Clinical Trials, among many other topics.

All this, in a comfortable 100% online mode that gives the student total freedom to organize their studies and schedules, without limitations of any kind. In addition, you can count on the most complete and up-to-date theoretical and practical content on the educational market, accessible from any device with an Internet connection.

Train your skills as a Monitor or Sponsor and achieve a promising future in one of the most promising areas in the veterinary field" 

This postgraduate certificate in Clinical Trials, Principal Investigator, Monitor and Sponsor 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 Principal Investigator, Monitor and Sponsor
• 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
• Practical exercises where self-assessment can be used to improve learning
• Its special emphasis on innovative methodologies
• 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

Thanks to its 100% online modality, the content will be available on the Virtual Campus from the beginning of the course, so you can enjoy it whenever you want"

The program’s teaching staff includes professionals from the sector who contribute their work 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 training programmed to train in real situations.

The design of this program focuses on Problem-Based Learning, in which the professional will have to try to solve the different professional practice situations that will arise throughout the academic course. This will be done with the help of an innovative system of interactive videos made by renowned experts.

You will have all the information you need to delve into Protocols, Reports and Investigator Interaction"

A program designed to help you achieve professional excellence in the veterinary environment"

The objective of this program is for the students to acquire the necessary skills and knowledge to be able to approach their professional future in these fields, with the highest quality and capacity in their work. All this, through the most complete and innovative practical and theoretical contents of the educational market.

Get to stand out as a Principal Investigator or Monitor, in a few weeks and without leaving home"  

General Objectives

• Generate specialized knowledge in the design and interpretation of a Clinical Trial 
• Examine the key features of Clinical Trials 
• Analyze key analytical concepts in Clinical Trials 
• Justify decisions made to solve problems 
• Evaluate behavioral aspects and standardized procedures of Clinical Trials 
• Review legislation on analytical, toxico-pharmacological and clinical standards and Protocols for veterinary drug testing 
• Assess the regulatory environment in relation to Clinical Trials  
• Develop standards for veterinary Clinical Trials  
• Generate specialized knowledge to carry out clinical research  
• Establish the correct methodology for conducting Veterinary Clinical Trials  
• Develop advanced knowledge for the development of a protocol for the conduct of a Clinical Trial with veterinary drugs 
• Analyze the structure of the different regulatory agencies and organizations and their attributions 
• Correctly manage the documentation generated in the framework of the application, follow-up and completion of a veterinary Clinical Trial 

Specific Objectives

• Generate a good clinical research Question 
• Plan an efficient, effective, and ethical design 
• Demonstrate that a Clinical Trial is feasible, efficient, cost-effective and easy to implement 
• Minimize errors (systematic and randomized) that may threaten the conclusions of a Clinical Trial 
• Generate specialized knowledge in clinical performance according to Evidence-Based Medicine 
• Encourage the search for scientific information, store it, evaluate it and use it through the use of computer applications 
• Critically evaluate how a scientific paper is reviewed 
• Synthesize ideas and analyze information in a critical, evaluative and analytical manner 
• Determine the role of each participant in the veterinary Clinical Trials research process, both in general and of the veterinarian in particular 
• Establish different roles in the research process and control of results 
• Examine factors and elements of the skills of actors in the testing process 
• Analyze the actions that guide the Clinical Trial process 
• Manage projects and Clinical Trials in scientific, technical and monitoring contexts 
• Determine the role and interests of the different stakeholders required 
• Analyze recruitment strategies for companies and researchers 
• Audit the research process and detect events of relevance to the progress of the research process 
• Issue partial, event and final reports 
• Decide on study sites and their monitoring 
• Ensure controls regarding data quality 
• Manage applicable legislation 

Master the different roles in the research process and control of results"