Entry Level Clinical Research Course

Drug discovery, Clinical Research, Clinical Data Management, Clinical Trial, Clinical Monitoring, GCP

What you'll learn

knowledge of drug discovery

Clinical research

Study design and protocol development

Ethical and regulatory considerations in clinical research

Data collection, management, and analysis

Requirements

Basic science knowledge

No experience in clinical

Description

This course is designed to provide a comprehensive introduction to the field of clinical research. Participants will learn about the key concepts and principles of clinical trials, including Good Clinical Practice (GCP), clinical trial design, study conduct, data management, and regulatory compliance. The course will also cover practical skills in study coordination, site management, data analysis, and report writing.Objectives:Upon completion of this course, participants will be able to:Describe the purpose and process of clinical research and clinical trials.Explain the principles of Good Clinical Practice (GCP) and regulatory compliance.Design a clinical trial protocol and implement a study according to the protocol.Manage clinical trial sites and coordinate study activities.Analyze and interpret clinical trial data.Write clear and concise study reports.Apply ethical and legal considerations in clinical research.Format:The course will be delivered through a combination of videos & articles.Assessment:Participants will be evaluated through an objective-question exam. Participants will receive a certificate of completion upon finishing the course and successfully passing the exam.Students have an opportunity for a 150 hours paid internship along with international industry certification to further enhance their skills and gain hands-on experience in the field. Students who are interested in internships can email us with their course certificates.Prerequisites:There are no specific prerequisites for this course. However, a background in the health sciences or a related field is desirable.Target Audience:This course is suitable for individuals who are interested in pursuing a career in clinical research, as well as health professionals and researchers who want to learn more about the process of developing new treatments.

Overview

Section 1: Importance and Scope of Clinical research

Lecture 1 Importance of Clinical research

Lecture 2 Introduction of clinical research

Lecture 3 Career scope in clinical research

Lecture 4 Career scope in clinical research

Lecture 5 Who can do career in clinical research?

Lecture 6 Who can do career in clinical research?

Lecture 7 Job Opportunities in the field of clinical research

Lecture 8 Job opportunities in the field of clinical research

Lecture 9 Who can hire clinical research professionals?

Lecture 10 Who can hire clinical research professionals?

Section 2: Overview of the clinical research process

Lecture 11 Drug discovery Process

Lecture 12 Theory of Drug discovery process

Lecture 13 Drug discovery to clinical research

Lecture 14 Theory of Drug discovery to clinical research

Lecture 15 WHAT IS CLINICAL RESEARCH?

Lecture 16 What is clinical research theory?

Lecture 17 IMPORTANCE OF CLINICAL RESEARCH

Lecture 18 IMPORTANCE OF CLINICAL RESEARCH

Lecture 19 Rational of clinical research

Lecture 20 Rational of clinical research theory

Lecture 21 Reporting and presenting clinical research findings

Section 3: History of clinical research

Lecture 22 The History of Clinical Trials

Lecture 23 The History of Clinical Trials: From James Lind to Nuremberg

Lecture 24 Nuremberg code

Lecture 25 Declaration of Helsinki

Lecture 26 Kefauver-Harris

Lecture 27 Belmont report

Section 4: Different stakeholder in clinical research

Lecture 28 Different stakeholder in clinical research

Lecture 29 Stackholders in Clinical Research

Section 5: Clinical Study design and protocol development

Lecture 30 Study design and protocol development

Lecture 31 Study design and protocol development theroy

Lecture 32 Data collection, management, and analysis

Lecture 33 Data collection, management, and analysis

Lecture 34 Data collection in clinical trials

Lecture 35 Data collection in clinical trials theory

Lecture 36 Data management and analysis

Lecture 37 Clinical trial monitoring and quality assurance

Lecture 38 Clinical trial monitoring and quality assurance

Lecture 39 Electronic Data Collection Methods

Lecture 40 Statistical Software and Data visualization tool used in clinical trial

Lecture 41 Regulatory Requirements For Conducting Clinical Trails

Lecture 42 current trends and future directions in the field of clinical research

Section 6: Clinical Research Focus

Lecture 43 Swalife Clinical Research Focus

Lecture 44 Diagnostic Studies

Lecture 45 Screening studies

Lecture 46 Observational Studies

Section 7: Exam

Lecture 47 Congratulation

Scientist curious about clinical research,Beginner in clinical research