Torrent Pharma owes its success in the domestic market to its thrust on frontline research, strategic marketing and world-class manufacturing. It is among the largest spenders on R&D and has set up one of the most advanced research centers in the country at an investment of Rs. 200 crores so far. It has discovered and patented the AGE (Advanced Glycosylation End Product) Breaker Compound which has potential to treat heart diseases and diabetes related vascular complications. Its manufacturing facilities have received quality certifications from various international regulatory authorities.
Role & responsibilities
Prepare and review study related documents i.e. Protocol, ICD, CRF and related all other documents are part of regulatory submission
Performing medical writing activities that support preparation of clinical study and regulatory documents required for drug development and registration activities
Performing Project Coordination, Project Planning and its Execution and Management
Preferred candidate profile
Qualification : M. Pharm with 2-5 yrs of relevant experience
Interested candidates can share their CVs on vilshashah@torrentpharma.com
