MBBS

Agricultural biotechnology, Food Biotechnology, Nutrition Biotechnology, Plant Molecular Biology, Bioinformatics, Nanobiosciences, Post-harvest technology, Functional foods, Genomics and Computational Biology.

Provide comprehensive statistical support across all phases of research studies, including clinical trials and epidemiological investigations, from design and sample size estimation to data analysis, interpretation, and reporting. Expertise in Clinical Research Methods, including study design, biostatistics, research ethics, and regulatory requirements. 

Life Science graduate with Masters in Hospital administration, Health Management with one year experience in Public Health, Hospital Administration. Candidates with experience in Healthcare Quality/formal quality of a quality system would be preferred.

5 years in a managerial position and has handled R&D projects independently viz. PI or Co-PI of Scientific studies, Head of Research Groups, Centres, Institutes, Laboratories, including experience in Child Health Research

BPharm/MBBS/Integrated BS-MS/MSc/BE/BTech or equivalent degree. Study of two-dimensional material interfaces for accumulated charge states for molecular interaction for self-powered gas sensor. To carry out experiments, characterizations, preparing reports etc. Instrumentation and Applied Physics, Indian Institute of Science, Bangalore

Position in the research project Centre for translational research and training on endocrine pancreas and Type 2 diabetes in India. M.Sc,BS-MS,M.Tech in Bioinformatics, Computational Biology, Systems Biology, Biotechnology OR BPharm, MBBS,B.Tech,M.Tech Computer science

Sepsis- related mortality in neonates in India, A multi-disciplinary, multi-institutional research program for context -specific solutions; As an academic Clinical Research Unit, to undertake & provide end -to- end clinical study support for investigators and SMEs in study planning, set up, conduct. project management, monitoring, data management, safety reporting, analysis and report writing

Contributes, with appropriate oversight, to all relevant aspects of global clinical trial activities to deliver study outcomes within schedule, budget, quality, compliance and performance standards. May lead specific aspects of global clinical trial. High quality contributions to study documents e.g. protocol, ICF, clinical sections of CTA -Clearly demonstrates Novartis Values and Behaviors i.e. Innovation, Quality, Collaboration, Performance, Courage and Integrity.

The WISE-IPR programme a programme of the Department of Science and Technology offers training in different fields of Intellectual Property Rights. This one- year training programme provides theoretical knowledge of IPRs as well as on-the-job training at various centers in the country.