Job Summary

• The role involves global leadership of pharmacovigilance processes to ensure compliance with worldwide regulations across Sandoz business units.
• Candidates will be responsible for managing adverse event handling for both post-marketing activities and clinical trials while ensuring data quality.
• The position requires leading audits, maintaining inspection readiness, and managing direct reports to deliver continuous operational goals.

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Skills & Requirements

Key Requirements

• Critical negotiations and people challenges experience
• Operations management and execution expertise
• Collaborating across boundaries capability
• People leadership and team management skills
• Clinical trial and databases proficiency

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