MBBS

Providing balanced, objective, and accurate information to regulators, the scientific community, health care professionals, payers, and patients in a consistent and timely fashion across the entire drug development lifecycle is fundamental to Lilly.

Masters Degree / PG Diploma in Life Sciences / Biomedical Sciences / Pharmacy / Public Health / Clinical Research with experience in clinical project management and/or clinical trial/ study monitoring.

Masters degree/ diploma, life sciences, pharmacy, public health, healthcare or other related discipline with a minimum of 2 years of relevant clinical trial monitoring or clinical trial/study coordinator, or clinical trial/study associate experience.

B.S. 4 years programme /BPharm/MBBS/Integrated BS-MS/MSc/BE/BTech or equivalent degree, with 55% marks and passing of NET/GATE test.

The minimum qualifications are BS 4 years programme, BPharm, MBBS, Integrated BS-MS, MSc, BE, BTech or equivalent degree, with 55% marks and passing of NET, GATE test.

Doctorate in life sciences or biomedical sciences or Pharmacy or Clinical Sciences OR Masters degree in life sciences or biomedical sciences or pharmacy or public health or clinical research

Post Graduate Degree including the integrated PG degrees in relevant subjects: Public Health, Health Economics, Epidemiology, Biostatistics, Pharmaceutical sciences, biomedical engineering

Post Graduate degree including the integrated PG degrees in pharmacology, public health, pharmacy,Biostatistics, statistics, Biotechnology or related disciplines with five years post qualification experience or PhD + two years post qualification experience

Post Graduate degree from a recognized University in Economics with specialization in Health Economics, Pharmacology, Pharmacy, Public Health, Biotechnology, Biostatistics