Clinical Research Essentials: A Beginner'S Blueprint

Unlock the Mysteries of Clinical Trials and Medical Research – No Experience Needed!

What you'll learn

Introduction to Clinical Research Overview Importance and Relevance

Understanding Clinical Research History, Regulations and Global Requirements

Dissect the importance of Drug Discovery in today's medical practice.

Learn the basics of clinical study design

Differentiate between the different clinical trial types and phases.

Understanding the importance of the different roles and responsibilities in clinical research conduct.

Requirements

No previous healthcare experience is required.

Description

Dive into the dynamic world of clinical research with our comprehensive course designed exclusively for beginners! "Clinical Research Essentials: A Beginner's Blueprint" offers a step-by-step guide to understanding the fundamentals of clinical trials and medical research processes. Whether you aspire to a career in healthcare, wish to join the pharmaceutical industry, or simply have a keen interest in science, this course is your gateway to mastering the basics.In this course, you will learn:Key Concepts of Clinical Research: Discover what clinical research entails and why it's crucial for medical advancements.The Design of Clinical Trials: Understand the methodologies behind setting up and conducting clinical trials.Ethical Considerations: Learn about the ethical standards and why they're essential in protecting study participants.Data Handling and Analysis: Gain insights into how data is collected, analyzed, and used to make evidence-based decisions.Regulatory Framework: Familiarize yourself with the regulatory environment that governs clinical research globally.Designed with the novice in mind, each module features easy-to-understand content supported by real-world examples, and additional resources to ensure a thorough learning experience. By the end of this course, you will not only gain a solid foundation in clinical research but also develop the confidence to contribute to life-saving research and perhaps even pursue further studies or career opportunities in this vital field. You will be skillful and qualified enough to apply the skills you have learnt in a Clinical Research Assistant role.Enroll in "Clinical Research Essentials: A Beginner's Blueprint" today and start your journey into the world of clinical research with confidence!

Overview

Section 1: Introduction To Clinical Research

Lecture 1 Overview of Clinical Research

Lecture 2 Importance and Relevance of Clinical Research

Lecture 3 Key Stakeholders in Clinical Research

Lecture 4 Ethical Considerations in Clinical Research

Lecture 5 Overview of Good Clinical Practice (GCP)

Lecture 6 Clinical Research Terminology For Non-Healthcare Professionals

Lecture 7 Introductions To Data Collection & Management

Lecture 8 Overview of Clinical Research Coordination

Section 2: Clinical Research Monitoring Visit

Lecture 9 Site Selection and Qualification

Lecture 10 Site Initiation for Clinical Professionals

Lecture 11 Site Staff Training and Oversight

Lecture 12 Understanding Complexity of ICF

Lecture 13 Monitoring Visit Coordination

Lecture 14 Role and Responsibilities of Study Visits

Section 3: Regulatory Compliance In Clinical Research

Lecture 15 Introduction to Regulatory Affairs

Lecture 16 IRB Ethics Committee Submissions

Lecture 17 Clinical Trial Protocol and Amendments

Lecture 18 Safety Reporting and Adverse Events

Lecture 19 Investigational New Drug (IND)

Lecture 20 Regulatory Environment in Clinical Research

Section 4: Quality Assurance and Quality Control In Clinical Research

Lecture 21 Audit and Inspection in Clinical Research Contexts

Lecture 22 Compliance and Quality Assurance in Clinical Research

Lecture 23 Data Falsification and Misconduct in Clinical Research

Lecture 24 Data Validation and Verification

Lecture 25 Quality Assurance and Quality Control

Lecture 26 Standard Operating Procedures for Clinical Research

Lecture 27 Understanding Audits in Clinical Research

Section 5: Clinical Research Patient Visits & Protocol Management

Lecture 28 ALCOA CCEA Principles of Documentation in Clinical Research

Lecture 29 Understanding Source Documentation In Clinical Research

Lecture 30 Protocol Deviation and Medical History Management

Lecture 31 Treatment Visit Day 7 Protocol Deviations and Adverse Event Updates

Lecture 32 Understanding the Baseline Visits In Clinical Research Protocol

Lecture 33 Understanding Study Protocols and Informed Consent

Lecture 34 Understanding Clinical Research Eliciting and Updating Health Records

Lecture 35 Understanding Adverse Events in Clinical Research

Beginners in clinical research and drug development,Non healthcare individuals interested in a career in clinical research.