Work as Pharmacovigilance Associate at Teva | M.Pharm, B.Pharm

Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation.

Post : Pharmacovigilance Associate II

Job Description
• Participate in activities of literature review and pre-signal detections
• Perform signal management activities related to Teva products
• Provide medical assessment for ICSRs associated with Teva marketed products
• Contribute safety related input to documents related to Teva products
• Participate in processing of post marketing cases
• Take part in databases search strategy discussions and be responsible for the data retrieval for safety assessment and evaluation
• Take part in providing medical safety information and assessment associated with marketed products to external and internal Teva stakeholders, mainly but not limited to:
• Clinical implications and health hazard associated with quality issues concerning generic products
• Health authority queries related to generic products
• Take part in preparing & providing training to newcomers or other MSU members in different topics as required

Candidate Profile
B.Pharm/M.Pharm/BDS/MDS/Equivalent life science education with 5-7 years of experience

Additional Information
Experience : 5+ years
Qualification : B.Pharm / BDS; M.Pharm/MDS
Location : Bangalore
Industry Type : Pharma / Healthcare / Clinical research
Functional Area : Regulatory Affairs
End Date : 25th March, 2021