Step into clinical research operations. Master GCP standards, trial coordination, and decentralized workflows for high-impact clinical trials.
Modular online course with applied concepts + mentor-led workshops
Beginner to intermediate
8 weeks
Conceptual + operational + real-world application
EDC systems, clinical documentation tools, AI coordination tools
Trial simulations, documentation exercises, operational workflows
Clinical Research, Trial Operations, GCP
Roles of Sponsor, CRO, Site, PI, and CRC. Trial lifecycle and ethics in clinical research.
GCP standards, Informed Consent, and participant rights. Inclusion/exclusion criteria and protocol adherence.
Regulatory binders, delegation logs, and TMF/ISF logic. Source vs CRF data integrity.
Screening workflows, visit calendars, and retention risks. Diversity and access in recruitment.
Monitoring visit preparation, query management, and handling deviations. CAPA protocols.
EDC systems, AE/SAE reporting, and remote visits. Decentralized trial (DCT) operations.
AI-assisted visit preparation and screening summaries. Documentation governance using AI tools.
Presenting site readiness to sponsors. Career transitions into CRC and CTA roles.
| Category | Launch Offer (INR) | Regular Price (INR) | International (USD) |
|---|---|---|---|
| Student | ₹9,999 | ₹14,999 | $350 |
| PhD / Researcher | ₹12,999 | ₹18,999 | $450 |
| Faculty | ₹13,999 | ₹21,999 | $500 |
| Industry Professional | ₹14,999 | ₹24,999 | $600 |
Become an industry-ready clinical operations leader with real trial management skills.
