Become a Clinical Research Associate in 8 weeks.
Live training for aspiring Clinical Research Associates. CT process and phases, monitoring visits, SDV and SDR, regulatory documents, CRF and TMF handling. Real monitoring-visit reports in your portfolio.
- Duration: 8 weeks
- Level: Beginner → Job-ready
- Live instructor-led: ₹28,000
- Self-paced: ₹10,000
Clinical Research Associate (CRA) curriculum
Module 01: Clinical Trial Basics
Phases, stakeholders, study design, roles of sponsor/CRO/site.
Module 02: ICH-GCP Deep Dive
E6(R2)/(R3) applied — sponsor vs site obligations, the real test.
Module 03: Essential Documents
TMF / ISF contents, regulatory binder, what counts as "complete".
Module 04: Site Selection & SIV
Feasibility, site qualification, initiation visit checklist.
Module 05: Monitoring Visits
SDV, SDR, visit reports (MVR) on real scenarios.
Module 06: Risk-Based Monitoring
Risk indicators, CTMS, central vs on-site monitoring.
Module 07: Protocol Deviations
PD handling, CAPA, audit and inspection readiness.
Module 08: Close-out + Placement
Close-out visit (COV), archival, resume review, interview prep.