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Clinical Research Coordinator (CRC) Cert...
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Curriculum
Clinical Research Coordinator (CRC) Certification
Overview of Clinical Research Coordinator (CRC) Course
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Introduction
03:38
Preview
Module 1: Introduction to Clinical Research
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Lesson 1: Introduction and History of Clinical Research
04:21
Assessment 1
4 questions
Lesson 2: Key Stakeholders in Clinical Research
05:21
Assessment 2
4 questions
Lesson 3: Clinical Trial Phases (Preclinical to Phase IV)
04:18
Assessment 3
4 questions
Lesson 4: Clinical Trial Designs
05:08
Assessment 4
4 questions
Lesson 5: Role and Responsibilities of CRC
05:06
Assessment 5
4 questions
Module 2: Regulatory Framework
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Lesson 1: ICH-GCP
04:08
Assessment 1
4 questions
Lesson 2: Overview of Regulatory Authorities
03:28
Assessment 2
4 questions
Lesson 3: Ethics Committee
05:51
Assessment 3
4 questions
Lesson 4: Key Regulations: 21 CFR Parts 11,50,54,56
06:26
Assessment 4
4 questions
Lesson 5: Informed Consent Process (ICP)
04:08
Assessment 5
4 questions
Module 3: Clinical Trial Process and Documentation
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Lesson 1: Site Selection and Feasibility Asssessment
06:06
Assessment 1
4 questions
Lesson 2: Essential Documents in Clinical Research
05:48
Assessment 2
4 questions
Lesson 3: Screening and Recruitment of Subjects
07:39
Assessment 3
4 questions
Lesson 4: Managing Patient Visits and Follow-ups
05:17
Assessment 4
4 questions
Lesson 5: Investigator Site File Maintenance
05:40
Assessment 5
4 questions
Lesson 6: Source Documents
05:44
Assessment 6
4 questions
Lesson 7: Archival of Documents and Reporting Study Results
05:23
Assessment 7
4 questions
Module 4: Communication and Coordination
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Lesson 1: Interaction with Stakeholders
05:47
Assessment 1
4 questions
Lesson 2: Handling Monitor Visits
06:23
Assessment 2
4 questions
Lesson 3: Patient Interaction and Retention
07:02
Assessment 3
4 questions
Module 5: Data Management and Safety Reporting
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Lesson 1: Basics of Clinical Data Management
06:21
Assessment 1
3 questions
Lesson 2: Data Query Resolution Process
05:28
Assessment 2
4 questions
Lesson 3: Adverse Events (AE) and Serious Adverse Events (SAE)
06:01
Assessment 3
4 questions
Module 6: Audits and Inspections
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Lesson 1: Preparing for Site Audits
06:08
Assessment 1
4 questions
Lesson 2: Common Findings in Audits and Inspections
05:42
Assessment 2
5 questions
Lesson 3: Regulatory Inspection Readiness
05:58
Assessment 3
4 questions
Module 7: Practical Insights and Terminologies
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Lesson 1: Case Studies
04:57
Lesson 2: Terminologies and Definitions for CRC
06:25
Assessment 2
4 questions
Final Assessment - Clinical Research Coordinator (CRC) Course
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Final Assessment CRC
40 questions
Video lesson
Introduction
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