Course Overview

This advanced program is for those seeking a comprehensive, in-depth understanding of the clinical research industry. It covers all fundamental aspects and dives deep into specialized domains, preparing you for leadership roles.

Building on the 3-month program, this course offers hands-on experience with advanced tools and real-world case studies from our parent CRO, giving you a competitive edge.

What You Will Learn

• All modules from the 3-Month Course
• Advanced Pharmacovigilance (Signal Detection, Risk Management)
• Hands-on Clinical Data Management with EDC Systems
• Medical & Protocol Writing (CTD/eCTD Dossiers)
• Global Regulatory Affairs (IND, NDA Submissions)
• Application of AI in Clinical Research & Data Analytics
• Professional Development (Soft Skills, Aptitude Q-Bank, HR Training)
• Live CRO Project Exposure

Key Features

• Live Project Exposure: Work on real, ongoing clinical trials.
• Case-Based Learning: Learn from actual industry case studies.
• Hands-On Training: Master essential skills in data management and regulatory documentation.
• Direct Mentorship: Learn from active CRO professionals.

Eligibility

Ideal for graduates and final-year students from Life Sciences, Pharmacy, and Medical or Allied Health fields.