At Knack Institute of Clinical Research, we offer specialized, practical training programs designed to equip you with job-ready skills in the field of clinical trials, pharmacovigilance, data management, and more.
Build Your Career with In-Demand Clinical Research Programs
Clinical Research
Learn how to plan, execute, and manage clinical trials.
Phases of clinical trials (I–IV)
Protocol writing, CRFs & ICFs
GCP, ICH, and ethical guidelines
Site selection, monitoring, and reporting
Pharmacovigilance
Monitor and manage drug safety to protect patient lives.
Adverse event reporting
Risk assessment and mitigation
Case processing using global databases
Post-marketing surveillance techniques
Medical Writing
Write clear, compliant, and scientific documents for global use.
Clinical study reports
Protocols, narratives, and summaries
Scientific articles and regulatory content
Language accuracy and structure formatting
Clinical Data Management
Master the process of collecting, cleaning, and validating clinical data.
Data capture tools (EDC systems)
Data validation and query resolution
Case report form design
Quality control and audit practices
Regulatory Affairs
Understand global regulatory systems and ensure product compliance.
Regulatory frameworks: USFDA, EMA, CDSCO
IND/NDA/ANDA filing procedures
Dossier compilation and review
Regulatory intelligence and documentation
SAP for Clinical Professionals (Part of Learning Program 3)
Bridge technology and clinical practice with SAP tools.
SAP interface for clinical operations
Trial tracking and workflow management
Dashboard analysis and reporting
Real-time project integration
Our Learning Programs
Learning Program 1
Foundation
16 Hours
Basics of Clinical Research, PDF Notes, Ideal for Beginners