FOUNDATIONS OF
CLINICAL RESEARCH MODULE

Overview

duration

Duration

4 weeks

format

Format

 Online, self-paced with interactive components

Empowering Clinical Research Knowledge

At Vlinkup, we provide comprehensive online training in clinical research, equipping participants with essential skills and knowledge to excel in the field and contribute to advancing medical science.

500
+

Participants

500
+

Trusted By Professionals

About Module

Foundations of Clinical Research

This four-week online, self-paced module provides a foundational understanding of clinical research. It covers essential topics such as the phases and design of clinical trials, regulatory and ethical requirements, and data management practices. Through a blend of readings, case studies, interactive quizzes, and group projects, participants will develop the knowledge and skills needed to navigate the clinical research process confidently. Completion of the module, including a final assessment, grants a certificate, making it ideal for healthcare professionals and researchers looking to deepen their understanding of clinical research fundamentals.

Module Objectives

By the end of this module, participants will be able to:

Weekly Breakdown

Week 1: Introduction to Clinical Research

  • Topics Covered:
    • Definition and Importance of Clinical Research
    • History and Evolution of Clinical Trials
    • Types of Clinical Studies: Interventional vs. Observational
  • Activities:
    • Readings from foundational texts
    • Interactive quiz to test understanding

Week 2: Clinical Trial Phases and Design

  • Topics Covered:
    • Overview of the phases of clinical trials (Phase I, II, III, IV)
    • Study Designs: Randomized Controlled Trials, Cohort Studies, Case-Control Studies
    • Sample Size Calculation and Statistical Considerations
  • Activities:
    • Case study analysis
    • Discussion forum on study design challenges

Week 3: Regulatory Requirements and Good Clinical Practice (GCP)

  • Topics Covered:
    • Role of Regulatory Agencies (FDA, EMA, etc.)
    • Introduction to Good Clinical Practice Guidelines
    • Informed Consent Process and Ethical Considerations
  • Activities:
    • Video lecture from an industry expert
    • GCP certification quiz

Week 4: Data Management and Reporting in Clinical Trials

  • Topics Covered:
    • Data Collection Methods and Tools
    • Importance of Data Integrity and Quality Control
    • Reporting Trial Results: Scientific Papers and Clinical Study Reports
  • Activities:
    • Group project to design a mock clinical trial
    • Peer review of trial designs

Assessment and Certification

Final Assessment

A comprehensive exam covering all topics discussed in the module.

Certification

Participants who successfully complete the module will receive a certificate of completion, validating their understanding of clinical research fundamentals.

Resources

Recommended Readings

List of books, articles, and journals relevant to clinical research.

Online Forums

Access to discussion groups for peer interaction and support.

Additional Tools

Access to templates for study protocols, informed consent forms, and data management plans.

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