Mock Interview Of Clinical Research Coordinator | Clinical Research Interview | 2023 #interview

Summary

In this video, the speaker reflects on their three months of experience in clinical research, highlighting their learnings and practical knowledge gained in areas such as protocols, case report forms, and clinical trial ethics. They also discuss their educational background in forensic science, personal strengths like being detail-oriented, and their drive to succeed in clinical research. Through various interview-style questions, the speaker explains the importance of trial protocols, ethical committees, investigator responsibilities, and trial monitoring. Despite early setbacks in securing a job in forensic science, they express confidence in their future in clinical research.

Takeaways

• 😀 The individual has been learning new concepts related to clinical trials over the past three months, including protocols, consent forms, and case report forms.
• 😀 They have a background in forensic science, having completed both their post-graduation and graduation at Helsing College in Karnal.
• 😀 The individual describes themselves as detail-oriented and well-organized, with confidence in handling challenges and delivering quality work.
• 😀 Their parents' professions are in business and boutique ownership, and they have one sibling in 12th grade.
• 😀 The concept of a 'protocol' is explained as a detailed, written description of a clinical study, including various key components like objectives, methodology, and statistical analysis.
• 😀 An Ethics Committee is a group responsible for ensuring the integrity and safety of clinical trials, protecting human subjects' rights.
• 😀 Two types of Ethics Committees are discussed: institutional and independent, with the latter focused on phase 4 studies and bioavailability/bioequivalence studies.
• 😀 Inclusion criteria for clinical trials are defined as the characteristics that participants must have to join the study, such as specific medical conditions, while exclusion criteria are those that disqualify individuals due to potential harm.
• 😀 An impartial witness is described as someone who ensures the consent process is fair and unbiased, helping to protect participant rights.
• 😀 Trial monitoring is emphasized as an essential part of overseeing clinical trials to ensure they follow protocols, regulatory requirements, and standard operating procedures, with different types of monitoring for pre-study, during-study, and closeout phases.

Q & A

What is the focus of the speaker's learning in the last three months?

The speaker has learned about new clinical trial rules, protocols, log books, informed consent forms, case report forms, and more, highlighting their involvement in the clinical research field.

What qualifications does the speaker have?

The speaker holds a post-graduation and graduation degree in forensic science from Helsing College, Karnal.

How does the speaker describe their working style?

The speaker describes themselves as a detailed, well-oriented person who can manage tasks efficiently, tackle challenges confidently, and consistently learn and improve their skills.

What does the speaker say about their parents' professions?

The speaker's father is a businessman, and their mother owns a boutique. They also mention having one sibling who is in 12th standard.

What is the purpose of a clinical trial protocol?

A clinical trial protocol is a complete written description and scientific rationale for any research activity involving human subjects. It includes details like study objectives, treatment period, inclusion and exclusion criteria, safety evaluations, and statistical analysis.

What are the two different types of Ethics Committees?

There are two types of Ethics Committees: Institutional Ethics Committees, which cover studies from Phase 1 to Phase 4, and Independent Ethics Committees, which approve only Phase 4 and BAB studies.

What is the importance of inclusion and exclusion criteria in a clinical trial?

Inclusion criteria define the characteristics a patient must have to participate in the trial, while exclusion criteria define characteristics that exclude patients to avoid harm or interference with the trial results.

What is the role of an investigator in a clinical trial?

The investigator is responsible for conducting the clinical trial, ensuring that all necessary facilities and staff are in place, recruiting suitable participants, maintaining data accountability, and adhering to ethical and regulatory guidelines.

What are the different stages of trial monitoring?

Trial monitoring includes pre-study, during-study, and study closeout phases. Pre-study ensures that the trial is ready, during-study monitors progress, and study closeout ensures all tasks are completed, documents are in order, and everything is ready for regulatory requirements.

How does the speaker view clinical research as a career?

The speaker finds clinical research to be a fascinating and growing field with great potential to contribute to society. They are motivated to pursue a career in this area due to its impactful nature.

What is the speaker's greatest weakness and how do they handle it?

The speaker's greatest weakness is their desire for clarity and perfection in their work. They feel uncomfortable when things are not perfect, though they understand that perfection isn't always achievable.

How did the speaker overcome their biggest career failure?

The speaker considers not being able to secure a job in forensic science after their post-graduation as their biggest failure. However, they now feel confident in their ability to pursue and succeed in clinical research.