Mastering Clinical Data Management: Learn and build a successful career in Clinical Trials and Research
Welcome to “Clinical Data Management (CDM) – The Ultimate Overview,” a comprehensive course designed for professionals and students eager to master the essential principles and practices of clinical data management. In the fast-paced world of clinical research, effective data management is crucial for the success of trials and the integrity of research findings.
What you’ll learn
- Fundamentals of clinical data management, including data collection, storage, and analysis.
- Regulatory Frameworks of Clinical Data Management.
- What are Clinical Data Management Plan.
- What are CRFs and how are they related to Clinical Data Management.
- What are Informed Consent Forms.
- Query Management in Clinical Data Management.
- Database Locking Procedures.
- How to develop a Statistical Analysis Plan.
- What is a Clinical Study Report.
- The trends and future of Clinical Data Management.
Course Content
- Introduction –> 2 lectures • 5min.
- The Basics of Clinical Data Management –> 9 lectures • 54min.
- Regulatory Framework and Ethical Considerations –> 3 lectures • 14min.
- Clinical Data Management – Planning Phase –> 3 lectures • 21min.
- Clinical Data Management – Data Collection & Entry Phase –> 3 lectures • 17min.
- Clinical Data Management -Data Cleaning and Validation Phase –> 7 lectures • 21min.
- Clinical Data Management – Data Integration and Analysis Phase –> 2 lectures • 11min.
- Clinical Data Management – Reporting Phase –> 1 lecture • 6min.
- Clinical Data Management – Post-Submission Phase –> 1 lecture • 4min.
- Current Trends and Technologies in CDM –> 2 lectures • 14min.
- Optional Section – Data Quality –> 13 lectures • 56min.
- Practice Test on Clinical Data Management –> 0 lectures • 0min.
- Course Closure –> 3 lectures • 7min.
Requirements
Welcome to “Clinical Data Management (CDM) – The Ultimate Overview,” a comprehensive course designed for professionals and students eager to master the essential principles and practices of clinical data management. In the fast-paced world of clinical research, effective data management is crucial for the success of trials and the integrity of research findings.
What You Will Learn:
- Fundamentals of Clinical Data Management: Understand the key concepts, terminology, and processes involved in CDM, including data collection, validation, and analysis.
- Regulatory Compliance: Gain insights into the regulatory landscape governing clinical trials, including Good Clinical Practice (GCP) and the role of regulatory authorities such as the FDA and EMA.
- Data Management Lifecycle: Explore the entire data management lifecycle, from study design and data collection to database lock and reporting, ensuring you grasp each critical step.
- Data Quality Assurance: Learn techniques for ensuring data accuracy and reliability, including data cleaning, validation checks, and audit trails.
- Technology in CDM: Discover the latest tools and technologies used in clinical data management, including Electronic Data Capture (EDC) systems and data analytics software.
- Practice: Practice your new skills with quizzes and practice tests.
This course is ideal for clinical research associates, data managers, biostatisticians, and anyone involved in clinical trials or interested in pursuing a career in clinical data management. Whether you are a beginner or looking to enhance your existing knowledge, this course provides valuable insights and practical skills.
Enroll today and take the first step towards mastering Clinical Data Management!