Masters in Life Sciences. Participate, as needed, on global teams to complete assignments and tasks within a specific task force/project associated with labelling
M.Sc, M.Tech, M.Pharm in Life, Biological, Allied life Sciences, Pharmacy. NET-JRF or LS, GATE qualified Two years experience in research and development in academic,industrial institutions
Masters degree, PG diploma, life sciences, pharmacy, public health, healthcare, or other related disciplines with a minimum of two 2 years of relevant clinical trial monitoring or clinical site coordinator experience.
M.Sc. Life Sciences or equivalent with minimum 60% marks in the qualifying exam. Candidates should be scholars who are CSIR-UGC NET or GATE qualified OR selected through National level examinations conducted by Central Government departments and their agencies or institutions
As Regulatory Professional, the candidate will be responsible for making the timely submissions to the Health Authorities worldwide. The candidate is expected to establish and maintain the CMC part of the core regulatory file. Further responsibilities include Life Cycle Management.
BS, RN, MS, PharmD in life sciences or equivalent relevant scientific qualifications or professional training. Generate and file data for signal detection and safety data review. Demonstrated understanding of global pharmaceutical drug development and lifecycles.
Overcoming the Inflammatory Cascade in Neonatal Sepsis, a Nanomedicine Approach. First class post-graduate PG degree including integrated PG degree such as M.S. Pharm, M.Pharm, M.Sc, M.Tech or Equivalent with specialization in Pharmacology & Toxicology, Regulatory Toxicology, Biotechnology, Life Sciences.
Masters degree in Life Science / Biochemistry / Biotechnology / Molecular Biology / Botany or any other branch of life science are eligible to apply. Genetic dissection of 13-lipoxygenases to modulate JA biosynthesis for enhanced N, P, K deficiency tolerance in rice