The M.Sc. in Co-vigilance & Clinical Research is a specialized postgraduate program designed to equip students with in-depth knowledge of drug safety, regulatory affairs, and clinical trial methodologies. The curriculum focuses on pharmacovigilance, medical writing, biostatistics, and ethical guidelines for clinical research, ensuring compliance with global regulatory standards.
This program is particularly relevant in the pharmaceutical, biotechnology, and healthcare sectors, preparing graduates for roles such as drug safety associates, clinical research coordinators, and regulatory affairs specialists. With the growing demand for safe and effective medicines, this field offers promising career opportunities in both industry and research settings.
M.Sc. in Pharmacovigilance & Clinical Research is promising, with opportunities in the pharmaceutical, biotechnology, and healthcare industries. Graduates can work in pharmacovigilance, ensuring drug safety by monitoring adverse effects and regulatory compliance. Clinical research roles involve conducting and managing clinical trials for new drugs and medical treatments.
Duration - 2 Years
Eligibility Criteria
B.Sc (Medical/Non Medical), B.Pharm and equivalent degree with 50% marks or equivalent grade.
Annual Fee - 1,00,000/-
Semester Fee - 50,000/-
Career Scope After M.Sc. Co-vigilance & Clinical Research
Career paths include Drug Safety Associate, Clinical Research Associate (CRA), Regulatory Affairs Specialist, Medical Writer, and Risk Management Specialist. Job opportunities exist in pharmaceutical companies, contract research organizations (CROs), regulatory agencies, hospitals, and academic research institutions. With experience, professionals can advance to managerial or senior scientific roles, contributing to drug development and public health. The growing global focus on drug safety and regulatory standards ensures steady demand for experts in this field.