Learn how Informed Consent is recorded from Clinical Research Courses?

How do patients usually arrive at the decision regarding informed consent?

In the process of informed consent, doctors or even professionals from the clinical research industry provide patients information on a specific test or treatment, Clinical research courses advice students on how they can suggest certain treatments or tests to patients. Once professionals give the patients this information, patients can then take a decision on whether they want to go ahead with the treatment or not. This is usually how the process of informed consent takes place and that’s why it is covered in a detailed manner in clinical research courses such that it is done in a proper manner.

What are the 2 ways in which consent is recorded?

There are 2 different ways in which the process of informed consent takes place and is recorded by professionals. Clinical research courses cover both procedures namely on paper and in electronic format. Apart from that, there are different components to confirm that participants have been provided with the necessary information and then have given consent.. The 2 ways are given below and professionals follow the procedures as specified in PG Diploma in Clinical Research:

1. Paper consent

Paper consent is collected in person by a professional from the participant of the study or trial.

2. electronic consent (eConsent)

Electronic consent or eConsent primarily uses hyperlinks, videos, and assessment tools to help with interpreting the consent document.

Yet, the professional still would confirm that the entire process of informed consent is complete with the assistance of other professionals. The information is usually reviewed by a physician or by researchers with appropriate scientific training and qualifications. Thus, it becomes essential for professionals to follow the rules effectively and they can learn the rules and regulations from clinical research courses.

Making the Process Simpler for the Participants

Most participants may not have a science or medical back ground hence they may ask a lot of questions. It is up to the professionals on how they make it simpler and that is why they should implement the suggestions given in clinical research courses.

Scope of Clinical Research:

India is the global hub of clinical trials. So, Many MNC’s are setting up research centers in India. This is because clinical trials and studies are an integral part of clinical research. Clinical research determines the safety and effectiveness of medicines, devices, and treatment. The safety and effectiveness of medicines and treatments are carried out before their availability in the market. Thus, there is a huge demand for trained clinical research professionals. The demand for professionals is not only in India but worldwide too. For example, Clinical Research provides excellent job opportunities in USA, Europe, Singapore and India. There are more than 2.5 Lakh opportunities worldwide in clinical research. Furthermore, the global clinical trials market size is expected to reach USD 68.9 billion by 2026. It is projected to expand at a CAGR of 5.7% during the forecast period. Therefore, there is a huge scope for clinical research in the coming years.

Career in Clinical Research:

Clinical Research carries out new research studies on human health, sicknesses and healthcare. Due to the exponential growth of the industry, there are several career opportunities in the clinical research industry. Once students finish their clinical research training programs, one can find lucrative job profiles in the industry. They are:

• Clinical Research Associate(CRA)
• Clinical Research Investigator(CRI)
• Business Development Manager
• Clinical Research Manager
• Medical Writer
• Data Manager
• Clinical Trial Auditor
• Project Manager
• Clinical Trial Writer

Sectors Where Candidates can find opportunities:

Candidates who have completed Clinical Research Courses / Pharmacovigilance Courses will be placed in the following sectors:

• Biotechnology Company
• Clinical Data Management Companies
• Pharmacovigilance Centers
• Pharmaceutical Companies
• IT Companies in Healthcare
• Central Laboratories
• Clinical CRO(Contract Research Organization)
• Data Management CROs(Contract Research Organization)
• Packaging Labeling and Contract Manufactures

I am Clinical Research Coordinator at TechnoBridge Systems.