The Advanced Diploma in Clinical Research is designed for individuals who want to build a strong career in clinical trials, drug development, and regulatory affairs. This program provides a deeper understanding of the scientific, ethical, and operational aspects of clinical research.
Topics Covered in the Program
In-depth study of ICH-GCP guidelines and regulatory frameworks
Clinical trial design, methodology, and protocol development
Roles of stakeholders: sponsors, CROs, ethics committees, investigators
Clinical data management and electronic data capture (EDC) systems
Pharmacovigilance, safety reporting, and SAE documentation
Regulatory submissions and audit preparation
Case studies and real-time project documentation
The focus is on industry-level training that aligns with global standards.
Who Can Join This Program
Graduates and postgraduates in life sciences, pharmacy, biotechnology, and medicine
Nurses, physiotherapists, and allied health professionals
Professionals working in healthcare or research wanting domain expertise
Students looking for job-ready qualifications in the pharma sector
Both freshers and experienced candidates can benefit from this course.
Career Roles After Completion
Clinical Research Associate (CRA)
Clinical Trial Monitor
Medical Writer (Clinical Documents)
Pharmacovigilance Specialist
Clinical Project Coordinator
Regulatory Affairs Executive
These positions are available in CROs, pharma companies, hospitals, and regulatory consultancies.