Masters in Clinical Research

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About Course

Master’s in Clinical Research course aims to provide students with a theoretical and practical understanding of the issues involved in the “Study design, conduct, monitor, document, audit, analysis and interpretation” of clinical trials of health interventions. It will be suitable for students working in high, middle and low income countries.

The various clinical research study modules of Diploma, Adv Diploma and PG Diploma courses taught in Single platform. M.Sc students may choose from a number of advanced modules which will have an opportunity to expand and deepen their conceptual and practical skills.

The main disciplinary perspectives will come from

  • Informed Consent Process
  • Ethics
  • Clinical Studies
  • Clinical Data Management
  • Data Analysis
  • Pharmacovigilance
  • Regulatory affairs
  • Epidemiology.

 

Students will be trained to develop skills to scrutinize information, to critically analyze and carry out research and to communicate effectively.

Duration : 2 years (4 Semesters)