Internship program MBA in Management and Monitoring of Clinical Trials

Degenerative diseases, cancer or the generation of new vaccines have focused scientific research and the creation of new medicines in recent decades. However, the great push in investment that came after the Coronavirus pandemic has highlighted the role of the pharmaceutical professional and investment in research. A reality that has led, in turn, specialists to seek to update their knowledge on the direction and development of Clinical Trials. This is why this 100% practical program was born, where the professional will spend 3 weeks in a specialized reference center together with professionals with experience in this field. A space where you can stay up to date with the latest news on the latest techniques and methods used in Clinical Trials.

University certificate

duration

3 weeks

Modality

On-site

Schedule

At your own pace

Exams

Online

start date

Credits

5 ECTS

financing up to

6 months

Price(first year)

See price

With this Practical Training you will take a definitive step in your career.”

Introduction to the Program

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”

Teaching Objectives

TECH has designed this Internship program to be able to offer professionals a practical and recent vision of the advances that are being produced in the monitoring of clinical trials. A stay where the specialist will be able to verify, together with experts from reference centers, how the teams in charge of carrying out research in said area are promoted and directed.

Update your professional profile with this 100% practical program in a real research center and assisted by experienced experts”

General Objectives

Master the latest techniques, modern scientific postulates and application of cutting-edge technologies in the Management and Monitoring of Clinical Trials
Know the specific approach to new drug developments
Incorporate the most effective methods, approaches and investigative analyzes into daily work, endorsed by a team of prestigious experts in the pharmaceutical sector

Specific Objectives

Explain the pharmacokinetic processes that a drug undergoes in the organism
Identify the legislation that regulates each of the steps in the development and authorization of a drug
Define the specific regulation of some drugs (biosimilars, advanced therapies)
Define the use in special situations and their types
Examine the process of financing a drug
Specify strategies for the dissemination of research results
Present how to read scientific information critically
Compile sources of information on drugs and their types
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)
Disclose the types of fraud committed in clinical trials research
Specify the different activities related to sample management (reception, dispensing, custody...) in which the Pharmacy team is involved

This Internship program will allow you to be up to date on the technical and administrative processes necessary in drug research in humans”

Internship Program in MBA in Management and Monitoring of Clinical Trials

The pharmaceutical industry is one of the largest sectors worldwide, not in vain its profitability has increased to such an extent that currently generates revenues of about 1.3 trillion dollars. Thanks to their massive production, today's medical treatments are more effective. However, the constant appearance of new diseases, added to the progressive strengthening of already known pathologies, has led specialists to develop numerous projects, studies and pharmacological research to face this problem. That is why the area of clinical trials stands out as one of the most relevant fields at present. For this reason, at TECH Global University we designed an Internship Program in Management and Monitoring of Clinical Trials, with which you will learn the technical and administrative processes necessary for the creation of new drugs. Through the study plan, you will have access to state-of-the-art scientific equipment, designed to provide you with the best educational experience. Through the lessons, taught in a medical center, you will learn the techniques of drug research and development, the protocols for monitoring the tests and the follow-up techniques for the patients who participate in the study.

Study a program on clinical trial management and monitoring

The legislative and regulatory regulations surrounding the management of clinical trials require specialized professionals who possess a high degree of experience and preparation. Therefore, in this TECH program, of only three weeks duration, distributed in classes of eight hours per day from Monday to Friday, you will learn the latest scientific-technical information on trial management and monitoring. Under the guidance of the best experts, you will learn about the steps involved in the development and authorization of a drug, its financing process, the dissemination of research results and sample management (reception, dispensing, custody). In addition, you will delve into the types of trials, good practice standards and protocols for drug research, authorization and differentiation. From this, you will gain the necessary skills to lead and/or supervise clinical trials, enabling you to achieve success and effectiveness in executed projects.