M.Sc, M.Tech, M.Pharm IPR from a recognized University. The incumbent should have sound knowledge of Patent Act, 1970 and should possess five years post qualification experience in dealing with issues like filling of Patent, Design, Copy Right & Trade Marks.
Tata Memorial Centre is an autonomous grant-in-aid institution of the Department of Atomic Energy. TMC is comprised of the Advanced Centre for Treatment, Research and Education in Cancer ( ACTREC) and the Tata Memorial Hospital ( TMH). ACTREC conducts a Ph.D. program in Life Sciences, affiliated to the Homi Bhabha National Institute (a deemed university under category A by MHRD, Govt of India). On-going research at ACTREC includes basic and translational research in Cancer Biology.
BHMS, BAMS, BUMS, BDS, B.Sc Life science, M.Sc Life Science, B.Pharma, D.Pharma and Diploma in Clinical Research. Preference will be given to the candidates having relevant experience in Clinical Research
PhD in Life Sciences, Computational Science, Bioinformatics, Genomics from a recognized University with minimum 6 months relevant post qualification research experience.
Ph.D. degree in life sciences or biotechnology equivalent from a recognized university with four years of post-qualification experience in the protein or vaccine development industry. OR MSc degree in Life Sciences or B.Tech degree in Biotechnology or equivalent from a recognized university
BSc in Life Science, B. Pharm. with PGDCR, Certification in Clinical Research OR MSc in Life Science, M.Pharm. with PGDCR, Certification in Clinical Research
Sun Pharmaceutical Industries limited is the largest specialty generic pharmaceutical company in the world. We provide high quality, affordable medicine trusted by healthcare professionals and patients in over ISO countries. It is also India's largest, most trusted and most valuable pharmaceutical company by market capitalisation.
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.