Advanced Diploma in
Clinical Research
This comprehensive 6-month online program is meticulously engineered to cover the full spectrum of Clinical Research, from Phase I to IV trials. Students will master protocol design, site monitoring, and rigorous ICH-GCP compliance. With a heavy emphasis on practical readiness, the curriculum integrates pharmacovigilance, clinical data management, and professional medical writing through hands-on projects, specifically designed to launch successful careers as Clinical Research Associates (CRA) or Coordinators (CRC).
Phase I-IV Expertise
Complete mastery of trial lifecycles, protocol design, and strategic site monitoring techniques for clinical excellence.
Compliance & Safety
Rigorous adherence to ICH-GCP guidelines and foundational training in global Pharmacovigilance safety standards.
Data & Documentation
Hands-on proficiency in Clinical Data Management and specialized Regulatory Medical Writing for global operations.
In collaboration with IBM
