Record and review adverse reactions in the safety database for post marketing and clinical trial reports in accordance with applicable regulatory standards, with high accuracy and quality.
Maintain safety tracking systems and ensure timely completion of assigned activities and deliverables. Conduct MedDRA coding, drug coding, and maintenance of drug dictionaries as required.
Ph.D degree in Microbiology/ Biochemistry/ Biotechnology subject from a recognized University with 2 years R&D/Teaching experience in the relevant subject after Ph.D
Bachelor of Pharmacy (B. Pharm) or Master of Pharmacy (M. Pharm) or B.Sc. Nursing or equivalent degree. U. N. Mehta Institute of Cardiology & Research Centre