TrialOps Pro: Clinical Trial
& GCP Operations
Step into clinical research operations. Master GCP standards, trial coordination, and decentralized workflows for high-impact clinical trials.
Format
Modular online course with applied concepts + mentor-led workshops
Level
Beginner to intermediate
Duration
8 weeks
Mode
Conceptual + operational + real-world application
Tools Used
EDC systems, clinical documentation tools, AI coordination tools
Hands-On
Trial simulations, documentation exercises, operational workflows
Domain
Clinical Research, Trial Operations, GCP
Program Curriculum
Clinical Research Ecosystem
Roles of Sponsor, CRO, Site, PI, and CRC. Trial lifecycle and ethics in clinical research.
GCP & Protocol Fundamentals
GCP standards, Informed Consent, and participant rights. Inclusion/exclusion criteria and protocol adherence.
Essential Documents & TMF/ISF
Regulatory binders, delegation logs, and TMF/ISF logic. Source vs CRF data integrity.
Recruitment & Participant Operations
Screening workflows, visit calendars, and retention risks. Diversity and access in recruitment.
Monitoring Readiness & Deviations
Monitoring visit preparation, query management, and handling deviations. CAPA protocols.
Data Flow & Decentralized Trials
EDC systems, AE/SAE reporting, and remote visits. Decentralized trial (DCT) operations.
AI for Clinical Operations
AI-assisted visit preparation and screening summaries. Documentation governance using AI tools.
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.