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Free Download Clinical Research Coordinator (CRC) Training Program (2026)
Published 8/2026
Created by Saurabh Kundgar
MP4 | Video: h264, 1920x1080 | Audio: AAC, 44.1 KHz, 2 Ch
Level: All Levels | Genre: eLearning | Language: English + subtitle | Duration: 15 Lectures ( 6h 15m ) | Size: 4.8 GB
Clinical Research Coordinator, Clinical Research, Good Clinical Practices, Trial Process, CRC Role & Responsibilities
What you'll learn
Introduction to Clinical Research Careers in Clinical Research, Data Management & Pharmacovigilance Drug Development, Phase trials & Regulatory Submissions Good Clinical Practices & 13 Principles of ICH GCP Fundamentals of Clinical Data Management Drug Safety & Pharmacovigilance Stakeholders in Clinical Research Role of Human Subject in Clinical Trials & Inform Consent Process Monitoring in Clinical Trials Roles & Responsibilities of Sponsor, Investigator, Site team in Clincial Trials Ethics Committee and Role in Subject Safety Protection Roles & Responsibilities of Clinical Research Coordinator, Clinical Trial Assistant & Clinical Research Associate Clinical Trial Design Blinding, Unblinding, Placebo & Randomization in Clinical trials Regulatory Submissions, Rules & Regulations Essential Documents in Clinical Research Terminologies for Adverse Events (AE), Adverse Drug Reactions (ADR) & Serious Adverse Events (SAE) & timelinesRequirements
No prerequisite is needed for this course.DescriptionBuild the knowledge and practical foundation you need to start or advance your career as a Clinical Research Coordinator (CRC).TheClinical Research Coordinator (CRC) Training Program (2026) is designed for students, graduates, healthcare professionals, life-science professionals, and aspiring clinical research professionals who want to understand how clinical trials are planned, conducted, documented, and regulated.
This comprehensive program takes you from thefundamentals of clinical research to the practical responsibilities of a CRC, helping you understand the clinical trial ecosystem, key stakeholders, regulatory expectations, essential documentation, and career opportunities.
You will begin with thehistory and evolution of clinical research, followed by the drug development process and the different phases of clinical trials fromPhase I through Phase IV. You will also develop a strong foundation inGood Clinical Practice (GCP) and the13 principles of ICH GCP.
The course then explores the roles and responsibilities of major clinical research stakeholders, including thePrincipal Investigator (PI), Sponsor, Ethics Committee (EC), Contract Research Organization (CRO), Clinical Research Coordinator (CRC), and clinical trial subjects.
A major focus of the program isclinical trial documentation. You will learn Good Documentation Practices (GDP) and understand essential documents requiredbefore, during, and after the conduct of a clinical trial.
You will also learn about theinformed consent process, major regulatory agencies governing clinical trials, and the importance of protecting clinical trial participants while maintaining data integrity and regulatory compliance.
Beyond technical knowledge, this program addresses an important question for anyone entering the industry
"How do I actually build a career in Clinical Research?"
You will exploreclinical research career opportunities, industry salary trends, growth and compensation insights, and practical strategies for starting your job search as a CRC.
What You Will Learn
By completing this course, you will develop an understanding of
Clinical research fundamentals and its historical evolution The drug development process Clinical trial phases I-IV Good Clinical Practice (GCP) The 13 Principles of ICH GCP Key stakeholders involved in clinical research Roles and responsibilities of the Principal Investigator (PI) Roles and responsibilities of the Sponsor Roles and responsibilities of the Ethics Committee (EC) Roles and responsibilities of Contract Research Organizations (CROs) Roles and responsibilities of the Clinical Research Coordinator (CRC) The role of clinical trial subjects The informed consent process Major regulatory agencies governing clinical trials Good Documentation Practices (GDP) Essential clinical trial documents Documents required before trial initiation Documents required during trial conduct Documents required after trial completion Clinical research career opportunities Industry salary, growth, and compensation trends Job-search strategies and best practices for aspiring CRCsWho Is This Course For?
This course is ideal for
Students pursuing Pharmacy, Life Sciences, Biotechnology, Medicine, Nursing, and related disciplines Recent graduates looking to enter Clinical Research Professionals planning to transition into Clinical Research Aspiring Clinical Research Coordinators Clinical Research professionals who want to strengthen their fundamentals Individuals preparing for CRC interviews and entry-level clinical research positions Anyone interested in understanding the clinical trial industry and career opportunitiesYour Career Starts With Understanding the Industry
Clinical Research is much more than conducting clinical trials. It is an industry built aroundpatient safety, scientific integrity, regulatory compliance, quality, documentation, and collaboration.
Whether your goal is to become aClinical Research Coordinator, Clinical Research Associate, Clinical Data Management professional, Regulatory Affairs professional, or pursue another clinical research career path, understanding the fundamentals is an important first step.
Enroll in theClinical Research Coordinator (CRC) Training Program (2026) and build a strong foundation for your journey into the clinical research industry.
Who this course is for
Students & Professionals exploring Career opportunities in Clinical Research Pharmacy graduates curious about Drug development & Clinical Trials Anyone curious about understanding Phase trials & Regulatory requirements Pharmacy, Biotechnology, Lifesciences, Chemistry & Medicine graduatesHomepage
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