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MSc. Clinical Research

Advanced training in clinical research, drug development, data analysis,
and evidence-based healthcare innovation.

MSc. Clinical Research

The M.Sc. in Clinical Research is a specialized postgraduate programme designed to prepare students for careers in the rapidly evolving field of clinical research and healthcare innovation. The programme combines scientific knowledge with practical training in the design, conduct, management, analysis, and reporting of clinical studies.

Students develop an understanding of how new medicines, therapies, vaccines, medical devices, and diagnostic technologies are evaluated for safety, efficacy, and quality. The programme emphasizes key areas such as clinical trial methodology, research ethics, regulatory affairs, pharmacovigilance, clinical data management, biostatistics, and evidence-based healthcare.

With India’s growing role in global clinical research, trained professionals are increasingly sought after by pharmaceutical and biotechnology companies, Contract Research Organizations (CROs), hospitals, academic research institutions, and regulatory organizations.

Graduates can pursue diverse career opportunities as Clinical Research Associates, Clinical Research Coordinators, Clinical Research Managers, Clinical Data Managers, Biostatisticians, Pharmacovigilance Professionals, and Regulatory Affairs Associates. The programme also provides a strong foundation for advanced research and higher academic pursuits in clinical and health sciences.

Eligibility Criteria

Candidates seeking admission to the M.Sc. in Clinical Research programme must meet the following eligibility requirements:

The M.Sc. in Clinical Research curriculum is designed to provide students with a comprehensive understanding of the scientific, clinical, ethical, regulatory, and operational aspects of clinical research.

Clinical Research Methodology

Fundamentals of clinical research, study designs, clinical trial phases, protocol development, and research planning.

Clinical Trial Management

Planning, coordination, monitoring, and management of clinical trials in accordance with established standards and procedures.

Biostatistics & Research Data Analysis

Statistical methods, data interpretation, clinical data analysis, and application of statistical tools in research.

Clinical Data Management

Data collection, database management, data validation, quality control, and ensuring the integrity of clinical trial data.

Regulatory Affairs & Ethics

Regulatory requirements, ethical principles, informed consent, research ethics committees, and guidelines governing clinical research.

Pharmacovigilance & Drug Safety

Detection, assessment, monitoring, and prevention of adverse effects and other drug-related safety concerns.

Evidence-Based Medicine

Critical evaluation of scientific literature and application of clinical evidence to support informed healthcare decisions.

Research Project & Practical Training

Hands-on exposure to clinical research practices through practical assignments, research projects, and industry or institutional training.

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