Your gateway to excellence in clinical research education

Join us on this transformative educational journey and unlock a world of opportunities in clinical research

We are an innovative educational technology company committed to empowering individuals with the knowledge and skills needed to thrive in the dynamic field of clinical research. Our comprehensive courses are designed to equip participants with the expertise required to make a meaningful impact on healthcare outcomes and advance the frontiers of medical science.

we understand the growing demand for qualified professionals in the clinical research industry. With advancements in medical treatments and the need for evidence-based practices, there has never been a better time to embark on a career in this exciting field


Our courses are meticulously crafted by industry experts and academic professionals to provide a comprehensive learning experience that combines theoretical knowledge with practical application

Medical Statistics

Courses in medical statistics equip researchers with the skills to collect, analyze, and interpret data from clinical trials and studies. Knowledge of statistical methods is vital for evaluating the effectiveness and safety of medical interventions.

Research Methodology

Research methodology courses cover the principles and techniques involved in designing, planning, and executing clinical research studies. Topics often include study design, data collection, ethical considerations, and research governance

Medical Ethics and Human Subjects Protection

These courses explore the ethical considerations and legal frameworks surrounding clinical research involving human subjects. They cover topics such as informed consent, patient privacy, and ensuring the welfare and rights of participants.

Data Management and Analysis

Courses in data management and analysis provide knowledge and skills in handling and analyzing clinical trial data. This includes data collection methods, database design, data cleaning, and statistical analysis techniques.

Clinical Trial Design and Management

This course focuses on the design and management of clinical trials, including the selection of appropriate endpoints, patient recruitment, randomization, and monitoring of trial progress. Understanding clinical trial regulations and Good Clinical Practice (GCP) guidelines is crucial.

Regulatory Affairs

Regulatory affairs courses provide insights into the legal and regulatory requirements for conducting clinical research. This includes understanding the processes for obtaining ethical approvals, managing informed consent, and complying with relevant regulations and guidelines.

Clinical Research Project Management

Project management courses focus on the planning, execution, and coordination of clinical research projects. They cover topics such as project planning, team management, budgeting, and timeline management.

Good Clinical Practice (GCP)

GCP training ensures researchers are familiar with the ethical and scientific standards required for conducting clinical trials. GCP guidelines outline the responsibilities of investigators, sponsors, and ethics committees in ensuring participant safety and data integrity.


Learn the vital role of pharmacovigilance in monitoring and ensuring the safety of pharmaceutical products. Understand the principles of adverse event reporting, signal detection, risk management, and regulatory requirements to contribute to patient safety in drug development and post-marketing surveillance.

Medical Writing

Develop expertise in medical writing, a critical skill in clinical research. Master the art of crafting clear, concise, and scientifically accurate documents such as clinical study reports, protocols, regulatory submissions, and patient education materials. Enhance your ability to communicate complex scientific information effectively

Medical coding

The Medical Coding course is designed for healthcare professionals seeking to enhance their skills in medical coding or embark on a career in this specialized field. Medical coding plays a crucial role in healthcare revenue cycles, ensuring accurate documentation, proper billing, and appropriate reimbursement. This course provides a comprehensive curriculum that covers the fundamental coding systems: ICD-10-CM, CPT, and HCPCS Level II.

Clinical research is the bridge that connects scientific discovery with improved patient care, paving the way for a healthier tomorrow.”

Take the first step towards a rewarding career in clinical research. 

Whether you aspire to become a Clinical Research Associate, Data Manager, Medical Writer, or Regulatory Affairs Specialist, our courses will provide you with the foundation and expertise to thrive in your chosen career path. Prepare to make a lasting impact on patient care, contribute to groundbreaking research, and shape the future of healthcare.

Job Opportunities:

Upon completion of our courses, participants can pursue a wide range of job opportunities in the clinical research field, including:

  • Clinical Research Associate (CRA): Monitor clinical trials, ensure adherence to protocols, and oversee data collection processes.
  • Clinical Research Coordinator (CRC): Coordinate and manage clinical research studies, including patient recruitment, data collection, and regulatory compliance.
  • Data Manager: Handle data management processes, ensuring accuracy, quality, and security of clinical trial data.
  • Biostatistician: Analyze and interpret clinical trial data, provide statistical support for research studies, and contribute to the design of clinical trials.
  • Medical Writer: Prepare clinical trial protocols, study reports, regulatory documents, and scientific publications.
  • Regulatory Affairs Specialist: Navigate regulatory requirements, manage submissions to regulatory authorities, and ensure compliance with regulations and guidelines.
  • Project Manager: Oversee the planning, execution, and coordination of clinical research projects, ensuring successful outcomes within timelines and budgets.
  • Drug Safety Specialist: Monitor and assess the safety profile of drugs throughout their lifecycle, including the detection, evaluation, and prevention of adverse events.
  • Pharmacovigilance Officer: Monitor and manage the safety and risk profiles of medical products, ensuring compliance with pharmacovigilance regulations.
  • Clinical Research Consultant: Provide expert guidance and support to organizations involved in clinical research, ensuring adherence to best practices and regulatory requirements.

Companies so far recruiting clinical researchers..





Omega Healthcare


HCL Technologies

Tech Mahindra

MModal Global Services

MiraMed Ajuba

.....and many more.


Join us on this transformative educational journey and unlock a world of opportunities in clinical research


Medical Writing

This course aims to equip participants with essential skills and knowledge required for proficient medical writing in clinical research. Participants will learn the principles and techniques of writing scientific manuscripts, regulatory documents, clinical study reports, and other essential documents. They will develop the ability to communicate research findings clearly, concisely, and accurately, following international standards and guidelines


Medical Statistics

This course aims to provide participants with advanced statistical knowledge and skills required for analyzing and interpreting data in clinical research. Participants will learn statistical methods used in clinical trials, observational studies, and epidemiological research, enabling them to make informed decisions and contribute effectively to evidence-based clinical practice



This course aims to provide participants with an in-depth understanding of pharmacovigilance principles, practices, and regulatory requirements in the context of clinical research. Participants will learn how to effectively monitor and evaluate drug safety data, detect adverse events, and contribute to patient safety throughout the drug development lifecycle.


Medical Coding

The aim of the Medical Coding course is to provide healthcare professionals with the knowledge and skills necessary to accurately assign medical codes for diagnoses, procedures, and services. The course aims to equip participants with the expertise needed to ensure proper documentation, billing, and reimbursement in healthcare settings.

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Are You a seasoned professional in the field of clinical research? Do you have a passion for sharing your knowledge and expertise with aspiring researchers? Join NSTC & get  the opportunity to make a significant impact on the next generation of clinical researchers.


Who can participate in these clinical research courses?

Our courses are designed for individuals who are interested in pursuing a career in clinical research or are already working in the field and seeking to enhance their knowledge and skills. We welcome students, graduates, healthcare professionals, researchers, and anyone with a keen interest in clinical research.

What are the prerequisites to enroll in these courses?

There are no specific prerequisites for most of our courses. However, a basic understanding of medical terminology and a background in life sciences or healthcare can be beneficial. Some advanced courses may require prior knowledge of specific subjects, which will be mentioned in the course descriptions.

Can I take multiple courses simultaneously?

Yes, you can enroll in multiple courses simultaneously if you wish to broaden your knowledge and skills across different areas of clinical research. However, please ensure that you can manage the workload and meet the requirements of each course.

What is the duration of each course?

The duration of each course varies. Most courses are designed to be completed within 3 to 6 months, depending on the depth of the content and the level of engagement required. The specific duration for each course will be mentioned in the course details.

Are these courses self-paced or instructor-led?

Our courses are primarily instructor-led, providing you with the guidance and support needed to maximize your learning experience. However, certain components of the courses may be self-paced, allowing you to study at your own convenience within given deadlines.

How will I be assessed during the course?

Assessment methods may vary depending on the course. They can include assignments, quizzes, case studies, group projects, and examinations. The exact assessment criteria will be provided at the beginning of each course.

Will I receive a certificate upon completion?

Yes, upon successful completion of each course, you will be awarded a certificate of completion. Our certificates are recognized and can add value to your professional portfolio.

Are these courses recognized by any professional organizations?

Our courses are designed to meet industry standards and are aligned with the best practices in clinical research. While they are not accredited degree programs, they are highly regarded within the industry and can contribute to your professional development.

Can these courses help me advance my career in clinical research?

Absolutely! Our courses are specifically designed to equip participants with the knowledge, skills, and practical insights needed to excel in the field of clinical research. By completing these courses, you can enhance your job prospects, pursue higher positions, or transition into new roles within the industry.

Can I get assistance or support during the course?

Yes, we provide continuous support throughout your learning journey. Our instructors and support staff are available to address any questions or concerns you may have regarding the course content, assignments, or technical issues.

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Don't miss your chance to be part of the next generation of clinical research professionals. Take the first step today by exploring our courses and enrolling in the program that aligns with your career goals


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