M.Sc. in Clinical Research at Padmashree Institute of Management and Sciences, Bengaluru/Bangalore

Padmashree Institute of Management and Sciences

M.Sc. in Clinical Research

Science (M.Sc.)

Shortlisted by 354+ Students

Location: Bengaluru/Bangalore

Duration: 2 YEAR

Regular / Offline

Average Fees: ₹ 1.50 Lakhs

Highlights The course offers a comprehensive blend of theoretical learning and hands-on training, covering key areas such as study design, trial conduct, monitoring, data analysis, regulatory affairs, and ethical considerations. With a strong focus on the scientific and operational aspects of drug development, the program equips students to contribute meaningfully to every stage of the clinical research process.

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Frequently Asked Questions

Career Prospects after M.Sc. in Clinical Research Course

Clinical research in India is evolving rapidly, especially with the growing involvement of regulatory authorities who are now actively shaping better systems and practices within the field. As a result of consistent efforts by industry leaders, regulatory guidelines in India are becoming more recognized and widely accepted, leading to a stronger focus on quality and compliance across the pharmaceutical sector. The introduction of the revised Schedule-Y has significantly influenced how clinical trials are designed and managed in the country, promoting higher standards and ethical practices. This shift is opening up promising opportunities for skilled professionals, making clinical research a thriving and future-ready career path in India.

Career Areas

Graduates of the MSc Clinical Research program find rewarding career opportunities across multiple domains within the clinical research industry. They are well-prepared for roles such as Clinical Research Associates, who play a key part in monitoring trials, or Clinical Trial Auditors, ensuring compliance and quality throughout the research process. Many also work as Clinical Research Investigators and Clinical Project Managers, overseeing the execution and management of trials. Other career paths include Data Managers handling trial data, Biostatisticians analyzing results, and Drug Safety Associates focusing on pharmacovigilance. Additionally, graduates can explore roles as Regulatory Affairs Managers, Medical Writers, and Business Development Managers, each contributing to different stages of the drug development and approval process. These diverse options reflect the program’s ability to equip students with both the technical and strategic skills needed in the fast-growing field of clinical research.

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