The Advance Diploma in Clinical Research is designed to equip students and professionals with in-depth knowledge of clinical trial protocols, ethics, data management, and regulatory frameworks. This program bridges academic learning with industry expectations, preparing participants for roles in clinical trial monitoring, coordination, and documentation.

Course Duration

🕒 9–12 Months

Placement Support

🎯 100% Placement Assistance with Clinical Research Organizations (CROs), pharmaceutical companies, hospitals, and healthcare research firms.

Program Highlights

• In-depth training in clinical trial phases, protocol design, ethics, and regulatory compliance

• Exposure to pharmacovigilance, biostatistics, and data management systems

• Practical modules aligned with ICH-GCP and global regulatory standards

E-Teaching Methodology

• 👩‍🏫 Live Faculty Sessions: Classroom and virtual sessions led by industry experts using real-world examples and presentations

• 📝 Assignments: Hands-on practice through CRF design, protocol drafting, consent form creation, and real case studies

• 🧪 Interactive Workshops: Focused training on SOPs, monitoring visits, adverse event reporting, and site initiation

• 📊 360° Evaluation: A performance-tracking system that evaluates understanding, skills, and professionalism

Eligibility Criteria

Who can apply:

• Graduates & postgraduates in Life Sciences, Medicine, Pharmacy, and Allied Health

• B.Pharm, M.Pharm, MBBS, BDS, BHMS, BUMS

• M.Sc / PhD / BA / MS in Biotechnology, Microbiology, Zoology, Chemistry, Biochemistry, Bioinformatics

• Nursing & Veterinary graduates

• Final-year students & professionals with relevant backgrounds

Bonus Career Module

• 📝 Resume Writing for Clinical Research Roles

• 🎯 Mastering Clinical Interview Rounds

• 🚀 Career Planning & Industry Entry Guidance