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Sanofi, through its iMove VIE Program, is seeking a Pharmacovigilance Associate to join the Pharmacovigilance & Safety team in Dubai. The role involves supporting local pharmacovigilance activities across the Greater Gulf region, ensuring compliance with local and global regulations, maintaining safety systems, and contributing to Sanofi’s mission to improve patient outcomes. This is a contract position under the VIE program targeted at EU citizens aged 18–28.
Key Responsibilities:
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Support local PV activities in compliance with regional, local, and global regulations.
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Collaborate with in-country partner functions and document processes in local Quality Documents.
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Manage compliance metrics, conduct Root Cause Analysis (RCA), and implement CAPAs.
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Ensure inspection readiness and maintain auditable trails of all PV activities.
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Complete CAPAs from audits or inspections and provide oversight via periodic reports.
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Monitor and interpret new or updated national PV regulations and forward to the regional PV team.
Requirements & Skills:
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Experience with pharmacovigilance systems and safety-related product management.
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Knowledge of international and local pharmacovigilance regulations and industry standards.
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Ability to interpret clinical and safety data effectively.
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Strong problem-solving skills, teamwork, and cross-cultural collaboration.
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Ability to work under pressure and manage multiple tasks.
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Proficiency in English (verbal and written); Arabic knowledge is a plus.
Education:
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Medical Doctor, Pharmacist, Pharm D, Veterinary Doctor, Health Sciences PhD, MPH, or Master’s in a related field.
Experience:
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Experience in pharmacovigilance, regulatory, quality, medical, or clinical development is required.
Contract & Work Arrangement:
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Contract under Sanofi iMove VIE Program
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Location: Dubai, UAE
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Target start date: 01/12/2025
