MBBS

Ph.D. from a recognized University in subject as given in a subject related to Reproductive, Child Health and Nutrition Experience of having worked in the area of management of reproductive health problems.

Post graduate degree in Life Science. OR Graduate, Post Graduate Degree In professional course e.g., M.Sc. Pharmacology, M.Pharm, MBBS,BDS selected through a process described through any one of the following Scholars who are selected through National Eligibility Test- CSIR-USG, NET including lectureship (Assistant Professorship) and GATE, GPAT.

M.Sc. in any branch of science e.g. Biology, Chemistry, Mathematics, Physics, M.Tech;, M B.B.S.. M.V.Sc.M.Pharm., Integrated M.Sc.. or equivalent qualification as per the norms of the Regional Centre For Biotechnology RCB, Faridabad, Haryana.

Lead the design, planning, and execution of clinical research studies, ensuring adherence to regulatory standards and research protocols. Focusing on understanding of the fetal and maternal health. 

B.S. 4 years programme /BPharm/MBBS; Post Graduate Degree in Basic Science or Graduate, Post Graduate Degree in Professional Course; Molecular and functional studies on LNCRNA-Guided regulation of replication stress response and genome integrity in mammalian cells.

As the project is in its ending phase most of labwork is completed. Hence, Good manuscript writing skills and computer knowledge with knowledge of statistical analysis is required.

05 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 related to Reproductive, Child Health or Nutrition

BPharm, BSc, MPharm, MSc, MBBS, BAMS; Experience in PV/ Clinical Research drug safety preferred. Ability to understand and analyses the complex data and performs the activities including accessing the case in Argus, code and enter data.

handle R&D projects independently in the areas of epidemiology, big data analytics, drug/ target/ biomarker discovery, preclinical and clinical evaluation of medical devices, IVDs, therapies, vaccines, field feasibility studies of the novel interventions, and experience/ exposure to regulatory aspects of health technologies, IP protection, Technology transfer. Health policy development and implementation. MD, MS or equivalent degree recognised by MCI, NMC OR MBBS or equivalent degree recognized by MCI, NMC, with MPH from a recognised university OR M.Sc or MBBS or equivalent degree, recognised by MCI, NMC, with Ph.D. from a recognised University.