Experteer Overview
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In this role you will deliver pharmacovigilance and safety surveillance services to clients, ensuring timely, compliant deliverables across the product lifecycle. You work with cross-functional teams to coordinate case processing, analyze safety signals, and support risk management activities. You help improve procedures and templates to boost quality and reduce rework. You guide less-experienced colleagues and align client expectations with service standards. This opportunity offers meaningful impact in safeguarding health for people and animals while advancing regulatory excellence.
Compensaciones / Incentivos
• Deliver client engagements and safety deliverables within defined scope, quality, and timelines
• Coordinate case processing, documentation, and handoffs to ensure accuracy and compliance
• Analyze safety data, literature,



and information to support signal detection and assessment
• Support development and maintenance of risk management deliverables and regulatory documentation
• Recommend and implement process improvements to procedures, templates, and workflow controls
• Facilitate coordination with client stakeholders and internal partners to confirm requirements and maintain alignment
• Guide less-experienced professionals through standards and reusable ways xqbhyrx of working
Responsabilidades
• 4+ years of experience in pharmacovigilance, drug safety, epidemiology, risk management, scientific consulting, regulatory affairs, or related field
• Bachelor in Life Sciences
• Certification in pharmacovigilance, drug safety preferred
• Certification in regulatory affairs, clinical safety preferred
• Certification in quality management, auditing preferred
Requisitos principales
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📌 Senior Manager Regulatory Affairs (Madrid)
🏢 Cencora
📍 Madrid