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M.Sc. in Clinical Research M.Sc. in Clinical Research
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M.Sc. in Clinical Research (2 Years)

M.Sc. in Clinical Research is a comprehensive two-year programme designed for students pursuing careers in pharmaceutical development and healthcare innovation. The curriculum covers clinical trials, drug development, regulatory affairs, and ethical considerations through hands-on training with CROs, hospitals, and pharmaceutical companies. Students develop expertise in trial management, data analysis, pharmacovigilance, and regulatory compliance.

Graduates emerge as Clinical Research Associates, Regulatory Affairs Specialists, or Clinical Data Managers, equipped with theoretical knowledge and practical skills essential for conducting systematic medical research that transforms healthcare interventions and advances patient care outcomes.

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Course framework for Master of Science in Clinical Research degree program at MIT School of Bioengineering, Sciences and Research, MIT ADT University, Pune

Sem I

  • Biostatistics (4 credits)
  • Fundamentals of Clinical Research (5 credits)
  • Research Methodology (3 credits)
  • Concepts in drug discovery (4 credits)
  • Programming using Python (4 credits)

Sem II

  • Clinical Trials and site management (5 credits)
  • Statistical analysis (4 credits)
  • Data Management in Clinical Research (4 credits)
  • Basics of Regulatory Affairs (4 credits)
  • Elective: Regulatory writing and medical coding, Health informatics (3 credits)

Sem III

  • Bioanalytical techniques (4 credits)
  • Global Regulatory Framework and audits (4 credits)
  • Pharmacovigilance and Safety Monitoring (5 credits)
  • SAS Programming and electronic data capture systems (4 credits)
  • Elective: IPR and ethics in clinical research, Pharmacoeconomics (3 credits)

Sem IV

  • External/ Industry Project 20 credits

Benefits of the Course

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  • Industry-focused curriculum developed with CROs, hospitals, and pharmaceutical companies
  • Hands-on training through internships at Contract Research Organizations and healthcare facilities
  • Comprehensive exposure to clinical trials, drug development, and regulatory compliance standards
  • Expert faculty guidance with real-world experience in pharmaceutical and clinical research
  • Career pathways in Clinical Research Associates, Regulatory Affairs, and Data Management roles
  • Access to advanced software training, including SAS programming and electronic data systems
  • Strong placement support with established networks in the pharmaceutical and healthcare industries

Eligibility Criteria

  • Bachelor's degree in Life Sciences, Pharmacy, Medicine, or related fields with a minimum required academic percentage
  • Strong foundation in biological sciences with interest in pharmaceutical research and clinical trial methodologies

Career Prospects

Roles in clinical research, include Clinical Research Associate, Site Manager, and Drug Safety Associate.
Opportunities in regulatory affairs and medical writing, ensuring compliance and preparing clinical documentation.
Positions in clinical data management and biostatistics, focusing on trial data handling and analysis.
Careers in pharmaceutical companies and CROs, supporting drug development and clinical trials.
Entrepreneurial support through MIT-ADTU BIO’s incubation centre for clinical research startups.

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