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Job Description & How to Apply Below
This leadership role drives the expansion of safety services in a clinical research environment. You will manage key pharmacovigilance operations, ensuring compliance while enhancing operational efficiency and client satisfaction. Collaborating with cross-functional teams and scientific experts, you'll influence business growth and advance patient safety.
Key Responsibilities:
• Oversee clinical trial pharmacovigilance and SAE processing
• Ensure compliance with sponsor requirements and KPIs
• Lead investigator communications and safety report distribution
• Design post-marketing safety infrastructure and workflows
• Develop strategic roadmaps for global safety service expansion
Requirements:
• Advanced degree in relevant scientific disciplines
• 10+ years in drug safety and pharmacovigilance
• 5+ years in leadership roles within safety teams
• Expertise in clinical trial and post-marketing safety
• Strong knowledge of FDA regulations and ICH guidelines
Guide the growth of safety standards and operations as a Senior Director.
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Position Requirements
10+ Years
work experience
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