MBBS

B.S. 4 years programme, BPharm, MBBS, Integrated BS- MS, MSc, BE, BTech or equivalent degree, with 55% marks and passing of NET, GATE test.

B.Pharm. with MBA/M.Pharm. or equivalent with at least 55% marks or MBA in Pharmaceutical Management with at least 55% marks

Lead Medical Writer is responsible for the development and review of medical writing deliverables that support the clinical regulatory writing portfolio and train the junior writers.

Master degree in Pharmacology, Clinical Pharmacology, Pharmacy Practice, Clinical Research. OR Pharm.D, MBBS, BDS from a recognized University, Institute.

The applicant should possess an M.D./M.S./Ph.D. degree (M.D./M.S./M.D.S. or MBBS/BDS/MVSc./M.Sc./M.Pharma/M.Tech or equivalent with Ph.D. in health/biomedical research) with at least fifteen years of experience

Ensure compliance with global and local procedural documents and local implementation of Patient Safety objectives, policies, processes and procedures. 

Masters degree, Ph.D in Public Health, Epidemiology, Life Sciences. OR Health Care Management, Health Administration after MBBS, BHMS, BDS or any other medical professional course in health Science.

Join Novartis as a Regulatory Writer and contribute to high-quality clinical and safety documents supporting global drug submissions. Ideal for candidates with medical writing experience.

First class Post Graduate Degree in a Life Science, Biochemistry, Pharmacology, Microbiology, Biotechnology including the integrated PG degrees OR Second Class Post Graduate Degree including the integrated PG degrees with PhD.