Certificate course in Clinical Research

Overview

• This program prepares you for roles such as Clinical Research Associate, Data Manager, Clinical Trial Coordinator, and Medical Writer.
  Modules include:
• Clinical trial design (observational/interventional)
• GCP & ethics
• Biostatistics & trial data management
• Monitoring, documentation, and site management
  Emphasis is placed on practical case studies, trial monitoring, data analysis, and compliance with regulatory standards like CFR. A certificate is awarded upon completion, and live projects are part of training.

Eligibility

• Bachelor’s degree (or higher) in Science/Healthcare domain
• Basic proficiency in biology, medical terminology, and research methodology
• Some courses may admit high school graduates with relevant subjects

Minimum Education