This program is designed by industry experts for students and young professionals. The training provides in-depth knowledge about the Role of a CRA towards Source Documentation, Managing Trial Master File (TMF) and Basics of Tracking Records using Clinical Trial Management System (CTMS).

Our Programs are delivered in SIP model for convenience of student:

  • Self-Paced Individual Program (SIP)
  • Skill and Job Oriented Certificate programs, delivered as Self-Paced Online with project solutions.


Clinical Research


10 Days



Admission Requirements

Recommended: An Associate or Bachelor’s degree in Medicine, Nursing, Pharmacy, Public health Biology, Biochemistry, Biotechnology, Chemistry, Clinical Research, Biomedical engineering, Public health, Pharmacology, or toxicology, Medical Device & Technology, Psychology, Sociology and Healthcare Administration.


Please Email your resume to Human Resources to check on your eligibility. We will contact you. Qtech’s objective is to provide you the right career pathway and advancement required to meet your career goals. Qualified candidates will have the opportunity to avail of our Post Training Assistance (PTA Program) for getting prepared and finding jobs.

Learning Outcomes

  • We adapt guidelines followed by American-FDA (US Food and Drug Administration), European-EMA (European Medicines Agency) and Canadian-Health
  • Presentations with voice-over and detailed online material
  • Mix of quizzes for practice, quizzes as test, Discussion based questions and various job-related exercises, along with solutions.
  • Learn on-demand, upgraded content that helps you stay up do date.
  • Applying Concept into Real-time (Policies, governance and tools)
  • Earn a Course Completion Certificate to showcase in your resume


SOP Development
Source Documentation, Retention and Compliance
Trial Master File (TMF)
Trial Master File
Trial Master File (TMF) , QC Management
CTMS Track Recording

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