Clinical Data Management
About
Master the essential principles and practices of clinical data collection, validation, and analysis in compliance with GCP and regulatory standards. This course provides practical training on data management plans, CRFs, EDC systems, query management, and audit readiness—equipping you for roles in clinical trials, CROs, and pharmaceutical R&D.
- Understanding the Clinical Trial Lifecycle
- CRF Design and Annotation
- Data Standards and CDISC Compliance
- Data Cleaning and Query Resolution
- Audit Trails and Regulatory Inspection Preparation
- Integration with Biostatistics & Medical Writing
- Real-world Case Studies and Projects
Clinical Data Management
About
Master the essential principles and practices of clinical data collection, validation, and analysis in compliance with GCP and regulatory standards. This course provides practical training on data management plans, CRFs, EDC systems, query management, and audit readiness—equipping you for roles in clinical trials, CROs, and pharmaceutical R&D.
- Understanding the Clinical Trial Lifecycle
- CRF Design and Annotation
- Data Standards and CDISC Compliance
- Data Cleaning and Query Resolution
- Audit Trails and Regulatory Inspection Preparation
- Integration with Biostatistics & Medical Writing
- Real-world Case Studies and Projects
Overview
Flexible Online Learning
Study at your own pace with access to video lectures, downloadable materials, and interactive modules.
Fundamentals of Clinical Data Management
Learn the core concepts, lifecycle, and importance of CDM in clinical trials.
Regulatory Guidelines & GCP Compliance
Understand how to ensure data accuracy and integrity in accordance with ICH-GCP, FDA, and EMA standards.
CRF Design & Development
Create effective Case Report Forms (CRFs) tailored to clinical protocols and data requirements.
EDC Systems Training
Get familiar with leading Electronic Data Capture (EDC) platforms used in the industry.
Query Handling & Data Validation
Learn practical skills to manage discrepancies, resolve queries, and clean clinical data.
CDISC & Data Standards
Introduction to CDASH, SDTM, and ADaM formats for compliant data submission.
Real-world Projects & Simulations
Practice with mock clinical trial data and scenarios to build real job skills.
Career Preparation & Certification
Prepare for roles in pharma, CROs, and clinical research with a certificate upon successful completion.
Expert Support & Community Access
Get guidance from experienced instructors and engage with a community of learners through discussion forums and Q&A sessions.
Popular Clinical Data Management Courses
WHY CHOOSE SCIENCELIV
The Best Beneficial Side of ScienceLiv
Industry-Relevant Curriculum
Gain practical knowledge and skills aligned with current clinical research and pharmaceutical industry standards.
Unlimited Lifetime Access
Access course materials anytime, anywhere — revisit content and resources as often as needed, with no expiration.
Learn from Experienced Professionals
Be guided by seasoned clinical data managers and research experts with real-world industry insights.
TESTIMONIALS
What Our Students
Say About the Course
Learners from diverse backgrounds have experienced the impact of ScienceLiv’s expert-led training. From bridging the gap between academic knowledge and real-world application to gaining job-ready skills in clinical research, regulatory compliance, and data management, our learners have advanced confidently in their careers. They consistently highlight the flexibility, industry relevance, and practical value of our courses—proving that ScienceLiv is more than just a training platform; it’s a career partner in the healthcare and life sciences sectors.
Clinical Research Coordinator
Very Powerful
Excellent Service
Course Instructors
Dr. Sneha Reddy
Clinical Data Management Lead with a decade of expertise in EDC systems, and GCP-compliant data practices.
Mr. Karan Mehta
