Post graduation in Science (M.Pharma, Life Science Biotech, Zoology, Botany) with PG diploma in Clinical Research. Candidate must have experience of 3 or more years in monitoring or handling of interventional clinical trials (RCTs) (Preferable in Oncology).
Ph.D./ MD / MS / MDS or equivalent degree or having 3 years of research, teaching and design and development experience after MVSc / M.Pharm / ME / M.Tech with at least one research paper in Science Citation Indexed journal.
M.Sc. in Microbiology/ Biotechnology from a recognized University. Candidates having hands on experience in handling microbes, enzymes and fermentation techniques will be preferred.
Strong knowledge of Quality Agreement / Technical Agreement drafting and review. Practical experience in vendor risk assessment, approved vendor list management and periodic vendor requalification.