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Certificate in Certified Clinical Research Professional (CCRP)


This six-months certificate program, has been designed to learn research design concept, data collection, analysis, monitoring and case management protocols and also identify the roles and responsibilities of the different position within the clinical research processes. The curriculum is focused to enhance learning abilities at every stage of the clinical research process from writing grant proposals and launching new projects to analyze data and presenting results. Using a blended learning model that corporates online as well as in-personlearning methodologies, the program delves into the latest developments and best practices in clinical research to prepare participants to drive health care innovations and ultimately lead the field forward


  • Explore the latest advancements and best practices in clinical research
  • Understand the multitude of responsibilities that go along with clinical
    research leadership and how to apply them strategically
  • Delve into the complex world of research ethics
  • Study drug development
  • Investigate secondary analysis of clinical trials

Clinical research is a rapidly expanding field, creating exciting opportunities for
trained professionals.
Clinical research professionals work in a broad range of research settings

  • Academic health care
  • Government agencies and departments
  • Clinical research assistant and associate
  • Clinical trials monitor
  • Contract research organization
  • Research clinical trial units of the universities
  • Private companies, such as pharmaceutical, biotechnology and medical device firm

Eligibility Criteria

  • MBBS, DPT, Pharm-D, BDS, DOT, BSN, BSNS, BS-MLT, BS-SLP, BSPT, BSOT or Equivalent Qualification recognized by HEC

Duration of Program: 06 months
Type of Study: Blended Learning Program (Face to Face / Online)

Fee Structure


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