Program Curriculum
Module 1: Clinical Research Ecosystem
Roles of Sponsor, CRO, Site, PI, and CRC. Trial lifecycle and ethics in clinical research.
Module 2: GCP & Protocol Fundamentals
GCP standards, Informed Consent, and participant rights. Inclusion/exclusion criteria and protocol adherence.
Module 3: Essential Documents & TMF/ISF
Regulatory binders, delegation logs, and TMF/ISF logic. Source vs CRF data integrity.
Module 4: Recruitment & Participant Operations
Screening workflows, visit calendars, and retention risks. Diversity and access in recruitment.
Module 5: Monitoring Readiness & Deviations
Monitoring visit preparation, query management, and handling deviations. CAPA protocols.
Module 6: Data Flow & Decentralized Trials
EDC systems, AE/SAE reporting, and remote visits. Decentralized trial (DCT) operations.
Module 7: AI for Clinical Operations
AI-assisted visit preparation and screening summaries. Documentation governance using AI tools.
Module 8: Capstone & Sponsor Review
Presenting site readiness to sponsors. Career transitions into CRC and CTA roles.
Transparent Pricing
| 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 |
Ready to Coordinate?
Become an industry-ready clinical operations leader with real trial management skills.
Apply for Enrollment