Learning Outcomes

Introduction to Clinical Research

Regulatory Affairs in Clinical Research

Designing Clinical Trials

Clinical Data Management

Clinical Trial Protocols

Fundamentals of Clinical Research - Lesson Smmary

In this module, you learn about the different roles and responsibilities in clinical research and review the regulatory affairs to ensure compliance with the guidelines. We cover designing clinical trials, protocol and ethical considerations to achieve reliable scientific results before looking at the monitoring and auditing of clinical trials.

Ethics in Clinical Research

Quality Assurance in Clinical Research

Clinical Trial Monitoring and Auditing

Good Clinical Practice Guidelines

Clinical Trial Reporting and Documentation

Lesson Summary

In this module, you will learn vital principles that guide clinical research to protect participants' rights and well-being. We cover how to conduct proper research through monitoring and auditing clinical trials, including how to implement good clinical practice guidelines.

Understanding the Basics of Biostatistics

Project Management in Clinical Research

Risk-Based Monitoring in Clinical Research

Working with Clinical Research Vendor

Informed Consent and Institutional Review Board

In this module, you will learn how to collect and interpret statistical information related to biology and medicine for better understanding. We cover clinical research project management with risk-based monitoring before looking at the various clinical research vendors, informed consent and institutional review board.

Essentials of Clinical Research - Course Assessment

Learn about core principles, ethical considerations and good clinical practice in this free online training course.

Essentials of Clinical Research

Clinical research seeks to evaluate the safety and efficacy of treatments and medications. This course will expose you to the many stakeholders' roles and obligations and how to ensure compliance with the regulations and guidelines. For precise and reliable data, we use clinical trial design and data management. Investigate clinical trial protocols and ethical concerns to ensure the safety and well-being of participants.

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