Qtech-Sol Professional Development Center
Live Webinar — Free Registration

Clinical Trials Data Management (CDMT)

Master the CDM lifecycle: CRF/eCRF design, data collection & validation, query workflows, external data loading, reporting, database lock & archiving, and regulatory compliance — plus live Q&A.

Webinar Snapshot

Date
Tue, Feb 17, 2026;
Duration
60 minutes
Level
Beginner–Intermediate
Mode
Live Online (Google Meet)
Seats
Limited (first-come, first-served)
Certificate
Attendance Certificate

Webinar Preview

Aligned to CDISC, ICH-GCP, Good CDM practices. Case-based tasks included.

What You’ll Learn

  • Introduction to clinical trial data management: collection, validation, cleaning, reporting
  • Database systems: CRFs, eCRFs, data repositories, external data loading
  • Query management & data clarification forms
  • Patient-reported outcomes & remote data entry
  • Database locking & archiving processes
  • Regulatory compliance, SOPs, data security & confidentiality

Why Attend?

  • Free registration with certificate
  • Direct pathway to CDMT training enrollment
  • Hands-on insights into industry-aligned CDM practices
  • Interactive live Q&A with experts

Webinar Agenda (60 mins)

00:00–00:05
Welcome & outcomes
00:05–00:15
Role of CDM & data lifecycle fundamentals
00:15–00:30
CRF/eCRF design, repository & external data loading
00:30–00:45
Query management & data validation & cleaning
00:45–00:55
Database locking & archiving, reporting best practices
00:55–01:00
Q&A + next steps
[CDMT - USA]

“The training on query management and data validation made me more confident in handling discrepancies. I successfully applied these skills in my first CDM role.”

— Lauren B., San Diego, California, USA
[CDMT - Canada]

"The session on CRF/eCRF design and external data loading clarified complex workflows. It helped me transition from a CRA role into a Data Management position.”

— Nancy G., Vancouver, British Columbia, Canada
[CDMT - India]

“The examples on database lock, archiving, and regulatory compliance gave me clarity on end-to-end CDM tasks. I now feel prepared for a career in data management.”

— Satish P., Hyderabad, India

Application Form

Accepted: PDF, DOC/DOCX, TXT, RTF, images, XLS/XLSX
You’ll receive confirmation and the joining link via email after submission.

Meet the Instructor

Dr. Chandra Nate, PhD

Clinical Operations & CDM Expert · 25+ years in the Pharmaceutical Industry

Dr. Nate is a seasoned leader in Clinical Operations and Clinical Technology Systems with hands-on expertise in CTMS/eTMF, EDC/CDMS, Data Quality, Risk-Based Monitoring, SAS Data Analytics, Oracle and Veeva platforms, and Regulatory Compliance. He has trained and mentored professionals globally and specializes in job-ready CDM workflows.

Learning Outcomes

  • Understand full clinical data management lifecycle in trials
  • Apply ICH-GCP & regulatory compliance in CDM activities
  • Design CRFs/eCRFs & manage case report data flow
  • Integrate & manage external data sources (labs, vendors, EDC)
  • Perform data cleaning, validation & discrepancy resolution
  • Manage and track data queries efficiently
  • Prepare datasets for analysis, review & submission
  • Lock and archive trial databases securely
  • Ensure SOP adherence & inspection readiness
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