Qtech-Sol Professional Development Center
Live Webinar — Free Registration

Clinical Trials Projects (CRAP) – CRA Role-Based

Role-based project simulations for CRA, CRC, CTA, and CSM: site selection & monitoring, data QC, SAE reconciliation, RBM dashboards, TMF maintenance, and real case templates — with live Q&A.

Webinar Snapshot

Date
Mon, Feb 9, 2026; Thu, Mar 26, 2026;
Duration
60 minutes
Level
Intermediate
Mode
Live Online (Zoom)
Seats
Limited (first-come, first-served)
Certificate
Certificate of Attendance

Webinar Preview

What You’ll Learn

  • Role-based project work for CRA, CRC, CTA, CSM
  • Applying protocol & trial management in simulations
  • Site selection, initiation & monitoring exercises
  • Data review, CRF QC, SAE reconciliation
  • Trial master file maintenance & audits
  • Risk-based monitoring & project reporting
  • Hands-on templates & case scenarios

Why Attend?

  • Free registration with certificate
  • Direct pathway to CRAP program enrollment
  • Access to Resume Marketing Services (RMS)
  • Live Q&A with an industry expert
  • Project-focused simulations you can apply

Webinar Agenda (60 mins)

00:00–00:05
Welcome & outcomes
00:05–00:17
Overview of project simulations
00:17–00:29
Site selection & monitoring tasks
00:29–00:41
Data QC & reconciliation
00:41–00:55
Risk-based reporting & templates
00:55–01:00
Q&A + next steps

Aligned to real-world project work; hands-on case simulations included.

[CRAP – USA]

“The role-based simulations made TMF maintenance and SAE reconciliation finally click. I added these to my resume and secured interviews for CRA project roles.”

— Olivia D., Austin, USA
[CRAP – Canada]

“Hands-on monitoring templates and RBM dashboards helped me streamline site oversight. I’m now leading monitoring tasks more confidently.”

— Amelia R., Vancouver, British Columbia, Canada
[CRAP – Australia]

“The project scenarios connected theory to practice — especially data QC and visit planning. I’m prepared to step into CRA/CTA hybrid roles.”

— Arjun M., Pune, 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 Expert · 25+ years in the Pharmaceutical Industry

Dr. Nate is a seasoned leader in Clinical Operations and Technology Systems with hands-on expertise across CTMS/eTMF, monitoring, TMF, and regulatory compliance. He has trained and mentored hundreds of professionals, focusing on practical, project-ready skills for CRA/CRC/CTA/CSM roles.

Learning Outcomes

  • Translate CRA/CRC/CTA/CSM theory into practice
  • Perform site selection & initiation activities
  • Conduct monitoring visits & site quality checks
  • Apply SAE reconciliation & safety reporting
  • Maintain TMF accuracy & documentation
  • Coordinate site/vendor communication
  • Track timelines & performance metrics
  • Prepare project reports for sponsor/CRO
  • Ensure audit-ready inspection readiness
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