Program overview

Clinical Research (CR) builds a strong foundation in trial conduct, study documentation, and compliance expectations in regulated environments.

Curriculum

• Clinical trial lifecycle and ICH-GCP principles
• Study start-up, conduct, monitoring, and close-out basics
• Essential documentation, deviations, and CAPA practices
• Role orientation for site, sponsor, and CRO workflows

Certification & mode

Eligibility

B.Pharm, M.Pharm, Pharm D, life-science and healthcare graduates.

Career outcomes

• Confident understanding of CR workflows
• Improved documentation and compliance mindset
• Interview-ready responses for entry-level CR roles

Apply / enquire

Talk to our counsellors for eligibility guidance, batch planning, and fee support.