TrueschoTruescho
All Courses
Fundamentals of Good Clinical Practice: Prep and Personnel
Coursera
Course
Unknown

Fundamentals of Good Clinical Practice: Prep and Personnel

Novartis

Learn the fundamentals of preparing for clinical trials, focusing on the investigator and site personnel roles, good clinical practice, and regulatory requirements.

Unknown3 weeksEnglish14,123 enrolled

About this Course

Welcome to 'Fundamentals of Good Clinical Practice: Prep and Personnel'! This course is designed to introduce you to preparing for a clinical trial. This is Course Two in the Clinical Trial Teams series - the first course 'Introduction to Good Clinical Practice' provides background on what clinical trials are as well as the basic principles and practices of GCP. If you are new to the world of clinical research, we suggest starting your journey with Course One. In Course Two, we turn our attention to the conduct of clinical trials, exploring in detail the role of the Investigator and site staff throughout a study. Whether you are new to the field or seeking to refresh your knowledge, this course will equip you with the necessary understanding to begin to navigate the complex world of clinical research. The course is divided into several modules, each covering specific stages of a clinical trial. The modules include a variety of videos, a fictional case study and interactive quizzes to reinforce your learning. We are excited to embark on this learning journey with you as we delve into the world of Good Clinical Practice. Enroll now and start building a strong foundation in the conduct of clinical research!

What You'll Learn

  • Understand the clinical trial process and regulatory requirements
  • Describe the roles of investigator and site personnel in clinical research
  • Explain the basic principles of good clinical practice

Prerequisites

  • Recommended to complete Introduction to Good Clinical Practice course

Instructors

N

Novartis Learning

Topics

Research
Health
Public Health
Good Clinical Practices (GCP)
Institutional Review Board (IRB)
Clinical Research Ethics
Clinical Trials
Document Management
Informed Consent
Electronic Medical Record

Course Info

PlatformCoursera
LevelUnknown
PacingUnknown
PriceFree

Skills

البحث
الصحة
الصحة العامة
الممارسات السريرية الجيدة
اللجنة الأخلاقية
أخلاقيات البحث السريري
التجارب السريرية
إدارة الوثائق
Informed Consent
Electronic Medical Record

Start Learning Now