To have an oversight on CRO partners for outsourced studies by conducting oversight quality visits at sites if applicable, conduct regular meetings and seek regular updates on study progress.
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.
M.Sc. in Chemical sciences, Life sciences OR Master of Pharmaceutical Sciences in Pharmaceutical chemistry, Natural Products OR M.Tech in Biotechnology, Nanoscience and Nanotechnology.
Masters in Natural or Agricultural or Pharmaceutical Sciences/MVSc/Animal Sciences OR Bachelors degree in Engineering or Technology or Medicine from a recognized University
Ph.D. in any branch of Life Sciences. Proficiency in bioinformatics analyses for metagenomes, whole genomes with nanopore and Nanostring. Translational Health Science and Technology Institute
Ph.D. in any branch of Life Sciences from a recognized university. Candidate should have experience in protein purification, microbiology, molecular biology experiments. Translational Health Science and Technology Institute
PhD degree in life sciences with experiences in using different in silico based tools and data- bases design. Advanced Centre for Treatment, Research and Education in Cancer ACTREC