Clinical Research Essentials: A Beginner'S Blueprint
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.
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Last updated 4/2024
MP4 | Video: h264, 1920x1080 | Audio: AAC, 44.1 KHz
Language: English | Size: 3.30 GB | Duration: 6h 1m
Unlock the Mysteries of Clinical Trials and Medical Research - No Experience Needed!
MP4 | Video: h264, 1920x1080 | Audio: AAC, 44.1 KHz
Language: English | Size: 3.30 GB | Duration: 6h 1m
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.
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