The candidate should have completed a Ph.D. in any field of Life Sciences or Chemistry and have experience in the characterization of natural products, proteomics, mass-spectrometry, metabolomics, etc., are encouraged to apply.
Postgraduate in Clinical Research, Life Sciences with over 10 years of experience in clinical trials, demonstrating proven expertise in managing multicenter and global clinical studies across various phases, with a specialization in Nephrology.
Masters degree in Life Sciences, Biotechnology, Bioinformatics, Chemical Sciences or equivalent subject with strong academic record. The student qualified NET-LS/GATE will be given preference.
M.Tech/ M.E/ M.Sc in Biotechnology/ Biochemistry/ Microbiology/ Molecular Biology/ Life Sciences/ Environmental Biotechnology/ Environmental Science from a recognized university
Drive report timelines and escalate risks or delays to team leads or management. Collaborate with cross-functional stakeholders and external business partners to collect PASR contributions and compile into PASR template.
To perform genotyping of the candidate genetic variants, ELISA, LC-MS/MS, Routine sample processing, DNA extraction, Toxicity collection, Clinical data monitoring and entry in paper and electronic CRF, reports preparation, assisting in data analyses, and performing tasks assigned by PI.
M.Sc, Ph.D in any branch of Life Sciences, Chemistry or related field from a recognized university. Candidates with involvement in innovation/design or social entrepreneurship or social empowerment using science or technology are particularly encouraged to apply.
M.Sc. in Marine Sciences / Microbiology / Biotechnology / Life Sciences. The candidates have a good technical writing and event management skills. The candidates will have to work in field also.