The Master of Science in Clinical Research program provides in-depth knowledge of the clinical trial process — from drug discovery and development to post-marketing surveillance. Students gain expertise in research methodologies, Good Clinical Practices (GCP), biostatistics, and regulatory frameworks used globally.

Core Subjects Include:

• Fundamentals of Clinical Trials
• Pharmacology & Drug Development
• Research Methodology and Biostatistics
• Clinical Data Management
• Bioethics and ICH-GCP Guidelines
• Regulatory Affairs (FDA, EMA, CDSCO)
• Pharmacovigilance
• Project and Site Management
• Medical Writing and Communication

The course typically includes practical training, internships, and project work in collaboration with hospitals, CROs, or pharma companies.

📥 Eligibility Criteria

• Bachelor’s degree in Life Sciences, Pharmacy, Medicine, Nursing, BDS, BPT, or Allied Health Sciences
• Minimum 50% aggregate marks
• Some universities may require an entrance test or interview

Job Roles After M.Sc. Clinical Research:

• Clinical Research Associate (CRA)
• Clinical Trial Manager
• Regulatory Affairs Specialist
• Data Manager / Clinical Data Analyst
• Pharmacovigilance Officer
• Medical Writer
• Research Scientist
• Quality Assurance Executive

Industries Hiring Clinical Research Graduates:

• Pharmaceutical and Biotech Companies
• Clinical Research Organizations (CROs)
• Hospitals and Research Labs
• Regulatory Agencies (CDSCO, FDA, WHO)
• Health Tech Startups
• Academic Research Institutes

Further Study/Certification Options:

• PG Diploma in Pharmacovigilance or Regulatory Affairs
• Ph.D. in Clinical or Biomedical Research
• Certifications from ACRP, DIA, or SOCRA

🌟 Why Choose M.Sc. in Clinical Research?

• High-demand profession in pharma, biotech, and healthcare
• Global career opportunities with lucrative salaries
• Industry-aligned curriculum with hands-on exposure
• Plays a vital role in public health and drug safety