Global Program Safety Lead - CRM (Barcelona)

Global Program Safety Lead - CRM (Barcelona)

08 ago
|
Novartis
|
Barcelona

08 ago

Novartis

Barcelona

Experteer Overview
¿Tiene las siguientes habilidades, experiencia e impulso para tener éxito en este puesto? Descúbralo a continuación.
In this role you oversee the end-to-end safety strategy for priority programs, guiding risk management across development and lifecycle. You will lead safety governance within global teams, manage emerging safety issues, and coordinate with health authorities to turn insights into action. You partner with cross-functional leaders to embed safety considerations into development, labeling, and lifecycle decisions. This is a high-impact role shaping patient safety at scale within a leading pharmaceutical company.
Compensaciones / Beneficios
• Lead end-to-end safety strategy for assigned programs across development and lifecycle
• Serve as scientific safety leader within global program, clinical, and trial teams
• Proactively identify, assess, and manage safety signals from all relevant sources
• Chair and drive Safety Management Teams for timely safety decisions
• Own and deliver core medical safety documents with rigor and consistency
• Guide benefit-risk evaluations and safety positioning for regulatory submissions
• Act as primary safety contact for health authority interactions




• Partner cross-functionally to embed safety insights into development, labeling, and lifecycle decisions
• Ensure compliant documentation, tracking, and governance of safety activities
• Mentor and guide colleagues to strengthen medical safety capabilities
Responsabilidades
• Medical Degree or equivalent (preferred)
• PhD, PharmD or equivalent graduate level health care professional degree required
• 5+ years’ experience in pharmaceutical drug development within a integral organization
• 3+ years of postdoctoral, patient-facing clinical experience
• 2+ years of hands-on experience in drug safety/pharmacovigilance xqbhyrx or medical safety roles
• Proven expertise in benefit-risk evaluation and clinical safety assessment across development phases
• Experience preparing safety sections of regulatory submissions and periodic safety reports
• Strong track record of leading cross-functional, multicultural teams in a matrix environment
• Fluency in spoken and written English
Requisitos principales
• hybrid working options
• minimum 14 weeks paid parental leave
• insurance plans
• retirement plans
• wellbeing resources
• global recognition programs

📌 Global Program Safety Lead - CRM (Barcelona)
🏢 Novartis
📍 Barcelona

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