📘 Introduction
The Clinical Trial Study Design (CTSD) program builds mastery in designing robust, compliant clinical studies—from defining objectives and endpoints to randomization, blinding, schedules of assessment, sample-size rationales, and statistical considerations. Learners translate protocol concepts into practical, inspection-ready study documents that drive reliable data and ethical conduct across phases.
🎓 Education Eligibility
- Bachelor’s or Master’s in Life Sciences, Pharmacy, Nursing, Public Health, Biostatistics, or Allied Health.
- Professionals transitioning from CRA/CRC/CDM roles into protocol & design responsibilities are welcome.
🎯 Unlock Your Career Potential – Join Our Live Webinar!
🚀 Ready to take the next step in Clinical Research?
Our upcoming webinar gives insider insights, real protocol design case studies, and a clear roadmap to job-ready success.
What you’ll get:
- Discover how Clinical Study Manager (CTSD) training prepares you for protocol-centric roles.
- Learn about career pathways, tuition options, and Resume Marketing Services (RMS).
- Get your questions answered directly by our experts.
👉 Seats are limited – reserve your spot today and move closer to your dream career!
📌 Building Relevant Experience – CTSD Core Topics
- Protocol Foundations: Study objectives, hypotheses, endpoints, estimands, and alignment to ICH-GCP.
- Design Choices: Parallel vs. crossover, adaptive designs, dose escalation, randomization & blinding.
- Statistical Inputs: Effect size, variability, power & sample size rationale; analysis populations (ITT/PP/Safety).
- Operational Plans: Schedules of assessment, visit windows, data flow, and key risk indicators.
- Safety & Ethics: AE/SAE pathways, DMC charters, stopping rules, and consent alignment.
- Documentation & Quality: SAP alignment, protocol deviations handling, and inspection readiness.
🧭 RMS Support (Post-Training)
Accelerate your job search with Qtech-Sol’s Resume Marketing Services (RMS):
- Resume building and interview coaching
- LinkedIn optimization and recruiter outreach
- Job application tracking and HR narratives
- 1-on-1 mentorship and job referrals (where applicable)
⏱ Duration
16 Weeks / 380 Hours (Self-Paced Access via Qtech’s AI-Driven LMS). Extensions available upon request.
💰 Tuition and Payment Methods
Tuition Fee:INR ₹120,542.75
- Credit/Debit Card (Visa or Mastercard)
- UPI / PhonePe (Optional)
- Installment Plan: 2–3 payments – 8% Discount
- Full Payment in Advance: Receive 65% Early-Bird Discount
📌 Apply Now
💼 Job Titles to Apply After Training
- Protocol Designer / Clinical Trial Designer
- Clinical Study Manager (Design Focus)
- Clinical Research Associate (Protocol Implementation)
- Clinical Trial Analyst
- Clinical Trial Assistant