Course description

This intensive Clinical Research Training Course offers a comprehensive overview of the principles and practices governing clinical trials. Participants will acquire practical knowledge in pivotal areas such as Good Clinical Practice (GCP) guidelines, meticulous study design, paramount ethical considerations, and stringent regulatory requirements. The curriculum encompasses the entire research lifecycle, from initial protocol development to sophisticated data management and rigorous statistical analysis. Through a combination of didactic lectures, in-depth case studies, and practical hands-on exercises, participants will cultivate the requisite skills to effectively contribute to and competently manage clinical research projects, thereby ensuring the utmost safety of participants and the unwavering integrity of research data.


What will i learn?

Requirements

Frequently asked question

This course imparts the requisite knowledge and proficiencies for conducting clinical trials, encompassing regulatory frameworks, ethical considerations, and study design methodologies.

This program is ideally suited for graduates in life sciences, healthcare professionals, and pharmacists who aspire to a career in clinical research.

A bachelor's degree in a life science, medical, or a closely related discipline is generally required.

The curriculum includes comprehensive coverage of good clinical practice (GCP), regulatory affairs, study management, and data handling procedures.

The course duration varies, typically ranging from a few weeks to several months.

Yes, successful completion frequently culminates in the conferral of a professional certificate in clinical research.

Graduates are eligible for positions such as clinical research associates, study coordinators, or data managers.

Numerous institutions offer flexible online and blended learning modalities for this course.

₹0

Lectures

17

Skill level

Beginner

Expiry period

Lifetime

Experience

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Certificate

Advance Your Career with the Dalton Dirac Doctorate of Business Administration (DBA) from Dunster Business School

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Friquently asked questions(FAQs)

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Lorem Ipsum is simply dummy text of the printing and typesetting industry. Lorem Ipsum has been the industry's standard dummy text ever since the 1500s, when an unknown printer took a galley of type and scrambled it to make a type specimen book. It has survived not only five centuries, but also the leap into electronic typesetting, remaining essentially unchanged.

Lorem Ipsum is simply dummy text of the printing and typesetting industry. Lorem Ipsum has been the industry's standard dummy text ever since the 1500s, when an unknown printer took a galley of type and scrambled it to make a type specimen book. It has survived not only five centuries, but also the leap into electronic typesetting, remaining essentially unchanged.

Upcoming batch section

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Cohort Starts: 12th Jul 2025

10 Modules | Duration: 60 Hours

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