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Team Lead AR&RM Strategy

3 - 7 years

14 - 19 Lacs

Posted:6 hours ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

Summary
-Monitors and audits the company s drug, biologics or medical devices surveillance program including the intake, evaluation, processing and follow-up on adverse reports. Participates in the resolution of any legal liability and in complying with government regulations. Ensures accurate receipt, maintenance and assessment against product labeling. Reports events or reactions as required by regulatory agencies including adverse events data from clinical trials, spontaneous or solicited sources, periodic and experience reports. May provide trending and safety signal detection and assessment. Supports all clinical trial activity and post marketing.


About the Role

Major accountabilities:

  • Global and /or regional, cross-functional leadership of assigned pharmacovigilance processes across Novartis

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NOVARTIS
NOVARTIS

Pharmaceutical Manufacturing

Basel Baselstadt

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