Teva Pharmaceuticals Hiring Pharmacovigilance Associate Teva Pharmaceuticals

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Job Posting: Pharmacovigilance Associate II at Teva Pharmaceuticals


About Teva Pharmaceuticals

At Teva Pharmaceuticals, we are committed to making good health more affordable and accessible, helping millions worldwide lead healthier lives. As the world’s leading manufacturer of generic medicines and a producer of numerous products on the World Health Organization’s Essential Medicines List, we reach over 200 million people daily. Join us as we continue to make a difference with new ideas and innovative solutions.


Position Details

  • Position Name: Pharmacovigilance Associate II
  • Organization: Teva Pharmaceuticals
  • Location: Bangalore, India, 560052
  • Salary: ₹17.6 Lakhs per year
  • Experience: 5-6 years
  • Qualification: B.Pharm, M.Pharm, Pharm.D, Lifesciences

Responsibilities

TaskDescription
ComplianceEnsure team activities comply with industry standards, company policies, and SOPs through procedural updates and training.
Strategy DevelopmentParticipate in building strategies for global pre-authorization studies and define and execute Teva standards.
Medical EvaluationPerform medical evaluations and clarifications of clinical trial-related adverse events (AE) including narrative content, queries, coding, expectedness, seriousness, and causality with company summary/medical assessment as applicable.
ConsultationAct as a consultant or Single Point of Contact (SPOC) for case-related activities, maintaining a knowledge repository of process updates and changes in real-time.
Safety ReviewProvide aggregate reviews of safety information, including clinical data, to maintain oversight of Teva’s medicinal products’ safety profile.
Administrative SupportAssist in V-Safe related administrative and procedural activities, ensuring all tasks are performed in compliance with work instructions and GVP modules.
Data AnalysisEnsure quality data analysis for trending and prepare the team for process stabilization.
Regulatory ComplianceFollow internal reporting key performance indicators to ensure regulatory compliance.

Qualifications

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RequirementDescription
EducationGraduation/Post-graduation in registered life sciences.
ExperienceMinimum of 5-6 years in Pharmacovigilance in a Biopharmaceutical/CRO industry, including experience in a large international organization.
Special SkillsExperience with pre-marketing studies and clinical trial case processing is an asset. In-depth knowledge of international PV regulations.

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