MBBS

Conduct medical review of all trial subjects in assigned clinical trials to ensure high-quality, consistent medical data. Ensure patient safety and adherence to protocols, Good Clinical Practice, ICH Guidelines, local regulations, and SOPs.

M.Sc., M Pharm. B.Sc. Prepares / supports the preparation of highly complex scientific documents to meet highest quality standards. Initiates, implements and champions process improvement techniques.

Good understanding of medical affairs function. Understanding of local regulatory policy and industrys code of practice related to drug registration, pharmaceutical promotion and clinical research.

Master degree in Pharmacy, Clinical Pharmacology, Pharmacy Practice and Clinical Research. OR Pharm.D/MBBS/BDS from a recognized university/ Institute. 

Pharmaceutical Sciences B.Pharm/M.Pharm/ Pharm.D. INTERNSHIP PROGRAM for esearch scholar/project trainee shall be supporting the coordinator/management of the monitoring centers

MSc in Microbiology / Biotechnology / Biomedical Sciences / Life Sciences with experience in Microbiology/ Biotechnology/ Biomedical Sciences/ Mycology Laboratory.

BSc Nursing, B.Pharma / MSW or BSc with relevant experience, as well as relevant experience in the field of Health System Research. 

MSc Life Sciences with at least 60% marks in final exam and 3 years research experience or PhD in life sciences or MBBS with 3 years research experience.

B.S. 4-year programme/ B.Pharm/M.B.B.S./Integrated B.S.-M.S./M.Sc./B.E./B.Tech or equivalent degree, with 55% marks and passing of NET-LS/GATE test (with validity)