Qtech-Sol Professional Development Center

Live Webinar — Free Registration

Clinical Data Assistant (CDAA)

Launch your Clinical Data Management career: EDC/CDMS essentials, CRFs/eCRFs, data pipelines, cleaning & validation, query handling, basic statistics & reporting, and data privacy — plus live Q&A.

Webinar Snapshot

Date

Thu, Feb 5, 2026;

Duration

60 minutes

Level

Beginner–Intermediate

Mode

Live Online (Google Meet)

Seats

Limited (first-come, first-served)

Certificate

Attendance Certificate

Webinar Preview

What You’ll Learn

Overview of clinical trials: phases, purposes, interventional vs observational designs
Ethical & regulatory compliance: informed consent, IRBs, Good Clinical Practice (GCP)
Study endpoints, control groups, randomization & blinding
Data management systems (CDMS/EDC), CRFs/eCRFs, data collection pipelines
Data cleaning, validation, and comprehensive query management
Basic statistical concepts & tools; result interpretation & visualization
Reporting & documentation: generating compliant reports
Data privacy, confidentiality, secure storage & transfer practices

Why Attend?

Free registration with certificate
Direct pathway to CDAA training enrollment
Access to Resume Marketing Services (RMS)
Insights into industry-aligned CDM practices
Networking and interactive Q&A with experts

Webinar Agenda (60 mins)

00:00–00:05

Welcome & outcomes

00:05–00:17

Intro to clinical trials + ethics & regulations

00:17–00:29

CDMS/EDC systems, CRFs/eCRFs & study design basics

00:29–00:41

Cleaning, validation & query workflows

00:41–00:55

Basic statistics & reporting, data privacy & security

00:55–01:00

Q&A + next steps

Aligned to ICH-GCP & global CDM standards; role-based case tasks included.

[USA]

“Clear walk-through of EDC, CRFs, and query handling. I updated my resume with CDM tasks and landed my first interview.”

— Emma J., Boston, USA

[Canada]

“Data cleaning and validation examples were practical. I now document discrepancies and audit trails confidently.”

— Liam M., Vancouver, Canada

[India]

“The overview of privacy & security and reporting made daily CDM tasks much clearer.”

— Kavya S., Chennai, India

Application Form

First Name

Last Name

Phone

Highest Education

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Work Experience (Years)

Student Category

Webinar Date

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Country

Domain

Program Name

Resume Upload

Accepted: PDF, DOC/DOCX, TXT, RTF, images, XLS/XLSX

You’ll receive confirmation and the joining link via email after submission.

RMS Support Book 1-on-1 Call Download Program Catalog

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, LMS, 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 hundreds of professionals globally. Known for bridging technology with clinical trial execution, Dr. Nate specializes in empowering Clinical Data teams with job-ready, real-world skills.

Learning Outcomes

Understand clinical trial phases, structure, ethics & regulations
Apply ICH-GCP & CDM standards in daily tasks
Use CDMS/EDC platforms for accurate data entry & review
Manage CRFs & ensure proper source documentation
Perform data cleaning, discrepancy checks & validation
Track, resolve & document data queries effectively
Maintain data privacy, confidentiality & security compliance
Generate clear reports aligned with regulatory requirements
Support clinical teams in ensuring database lock readiness