This Internship program will update your daily practice in the area of Clinical Trial Monitoring, for 3 weeks in a reference health center” 

In recent years, the increase in infectious diseases and the pandemic caused by COVID 19 have led public and private institutions to adopt new formulas to enhance the I+D+i and retain talent in the field of research. This scenario opens up an excellent opportunity for pharmaceutical professionals who wish to update and expand their scientific-technical knowledge about the Management and Monitoring of Clinical Trials.

Faced with this reality, TECH has created this Internship program, which provides pharmaceutical professionals with a stay in a prestigious research center. In this space, the specialist will obtain an update on the techniques, methods and protocols used in the coordination and conducting Clinical Trials. A period where you will expand your skills together with a team of professionals with extensive experience in this field.  

Thus, over 3 weeks the student will become part of a team of top-level professionals, with whom they will actively work. In this way, you will be able to update not only the most effective strategies, but you will also be able to implement the most assertive communication skills and leadership skills into your praxis that will allow you the best practice in Management and Monitoring of Clinical Trials, in a scenario real and cutting edge.

This program provides you with a complete update of your knowledge in the field of clinical trial monitoring”

The Internship program MBA in Management and Monitoring of Clinical Trials made up of a stay in a reference research center. Moreover, for 3 weeks, the professional will remain, from Monday to Friday, working 8 consecutive hours alongside specialists with extensive experience in clinical trials.

A period where the professional will be able to update their knowledge and expand their skills in managing research teams. In addition, it will enhance its technical capabilities on the methods and protocols currently used in clinical trial monitoring processes.

In this training proposal, completely practical in nature, the activities are aimed at developing and perfecting the skills necessary for the provision of Clinical Research, conditions that require a high level of qualification, and are oriented towards specific training for the exercise of the activity, in a safe environment and high professional performance.

It is, without a doubt, an excellent opportunity to obtain a direct and practical vision in a space where research and scientific rigor go hand in hand. In this way, TECH offers a new way of understanding and integrating innovative processes through an experience that promotes the improvement of professional skills and competencies.

The practical teaching will be carried out with the active participation of the student performing the activities and procedures of each area of competence (learning to learn and learning to do), with the accompaniment and guidance of teachers and other training partners that facilitate teamwork and multidisciplinary integration as transversal competencies for medical practice (learning to be and learning to relate).

The procedures described below will be the basis of the practical part of the training, and their implementation will be subject to the center’s own availability and workload, the proposed activities being the following:

Research and Development of Medicines 

• Participate in the Develop from all phases of a clinical trial  
• Identify and know how to use the different drugs that can be used in clinical trials
• Collect clinical trial data for further analysis  
• Publish research results in different formats

Clinical Trials Coordination

• Provide support in the presentation of documentation for the implementation clinical trial underway
• Identify all the documents to be contained in the researchers file and managing 
• In the communication of the results of clinical trials through the most appropriate means in each case
• Manage and provide support in the global monitoring process  

Bioethics and regulations in development of Clinical Trials 

• Establish research protocols for Clinical Trials
• Carry out the whole process of clinical trials following the current legislation on the matter
• Participate in the Develop from a safety surveillance plan for marketed drugs
• Recognize and comply with the rules governing Clinical Trials

Follow-up of Patients in Clinical Trials

• Monitor patients participating in research projects
• Manage monitoring visits and closure of the clinical trial
• Collaborate in the Assess from the treatments and possible adverse effects caused by some drugs
• Participate in the Develop Clinical from Trials with the collaboration of the hospital pharmacist
• Ensure the safety of participants in Clinical Trials

Receive specialized education in an institution that can offer you all these possibilities, with an innovative academic program and a human team that will help you develop your full potential”