Master degree in Pharmacology, Clinical Pharmacology, Pharmacy Practice, Clinical Research. OR Pharm.D, MBBS, BDS from a recognized University, Institute.
M.Sc in Chemistry, Organic chemistry, Biochemistry, Pharmaceutical Chemistry, Microbiology, Human genetics, M.Pharma with pharmaceutics or pharmacology as one of the subjects
The Tata Memorial Centre (TMC) is a Comprehensive Cancer Centre with a mission to achieve the highest standards in patient care, cancer prevention, cancer research and professional development for oncology and allied disciplines. TMC is an autonomous body funded, controlled by the Department of Atomic Energy, Government of India. TMC is affiliated to Homi Bhabha National Institute (HBNI).
Ph.D. or equivalent degree OR three years of research, teaching, design and development after MVSc, M.Pharm, M.E, M.Tech with at least one research paper in Science Citation Index Journal.
An ability to read and understand diverse literature across the many disciplines relevant to drugs, nucleic acid delivery to distill the best new ideas in the field and apply them to your work. An ability to identify the challenges associated, bottle necks in development and suggest mitigation proposals during development at various stages.
B.Pharmacy OR 10+2 with science stream D.Pharmacy. ECHS Polyclinics Ahmednagar, Osmanabad, Latur & Beed for a period of one year renewable for additional period of one year.
Post Graduate Degree, including the integrated PG degrees, with five years post qualification experience or PhD plus two years post qualification experience.
Masters in Chemistry, Organic Chemistry, Medicinal Chemistry from a recognized University OR Any equivalent qualifications duly recognized by the concerned authority as per the functional requirement
Knowledge and experience in the international regulatory environment of clinical trial applications, non-clinical and/or clinical variations to marketing authorizations and product labelling relevant for biotechnology and/or oncology products
Role is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidances and defined regulatory strategies.