📘 Introduction
Qtech-Sol’s Clinical Data Management (CDM) program prepares you for roles where accuracy, compliance, and data integrity are paramount across the drug development lifecycle. Build in-depth knowledge of CDM processes aligned to ICH-GCP and sponsor expectations—covering CRF/eCRF design, edit checks, validation, query handling, database lock, and audit readiness with simulated industry systems.
🎓 Education Eligibility
- Bachelor’s or Master’s in Life Sciences, Biotechnology, Nursing, Pharmacy, Public Health, or related fields.
- Basic understanding of clinical trials or data processing preferred.
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🚀 Ready to take the next step in Clinical Data Management?
Get insider insights, real CDM case demos, and a clear roadmap to job-ready success.
What you’ll get:
- How CDMT training prepares you for industry roles.
- Career pathways, tuition options, and Resume Marketing Services (RMS).
- Get your questions answered directly by our experts.
👉 Seats are limited – reserve your spot today!
📌 Building Relevant Experience – CDM Core Responsibilities
- CRF/eCRF Design: Translate protocol into data fields and forms.
- Edit Checks & Validation: Specify rules; configure checks; ensure data accuracy.
- Data Entry & Discrepancy Management: Generate, track, and resolve queries.
- SAE Reconciliation: Collaborate with Safety to align clinical and PV data.
- Medical Coding: Apply MedDRA and WHO-Drug dictionaries effectively.
- Review & Audit Readiness: Listings, logs, and QC reports for inspections.
- Database Lock: Clean-file review through to lock simulation.
💻 Tools & Hands-On Practice
- Simulated CDMS for real-time data entry and validation.
- Excel-based trackers for edit checks, queries, and review logs.
- CDM SOP templates, Data Management Plans, and mock audit checklists.
📂 Documentation & Compliance
- Good Clinical Data Management Practices (GCDMP) guidelines.
- Data integrity, traceability, and audit trail compliance.
- ICH-GCP aligned workflows for global study execution.
🧭 RMS Support (Post-Training)
Boost your job search with Qtech-Sol’s Resume Marketing Services (RMS):
- CDM-focused resume & cover letter building.
- LinkedIn optimization and recruiter connections.
- Mock interviews and eCRF task walk-throughs.
- Guidance on CTMS/CDMS job portals and applications.
⏱ Duration
8 Weeks / 164 Hours (Self-Paced Access via Qtech’s AI-Driven LMS). Extensions available on request.
💰 Tuition and Payment Methods
Tuition Fee:INR ₹88,750.20
- Credit/Debit Card (Visa or Mastercard)
- UPI / PhonePe (Optional)
- Installment Plan: 2–3 payments – 50% Discount
- Full Payment in Advance: Receive 65% Early-Bird Discount
📌 Apply Now
💼 Job Titles to Apply After Training
- Clinical Data Coordinator
- Clinical Data Associate
- Clinical Trial Data Analyst
- Clinical Data Manager (Junior)
- eCRF Designer / Data Validator