ICON is a integral healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Pharmacovigilance Reporting Specialist at ICON, you will be responsible for the timely and accurate preparation of pharmacovigilance reports, ensuring compliance with regulatory requirements and internal policies.
What You Will Do:
You will contribute to pharmacovigilance and drug safety activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
- Preparing and submitting comprehensive safety reports, including periodic safety update reports (PSURs) and individual case safety reports (ICSRs), in compliance with regulatory standards.
- Conducting thorough data analysis to identify trends and assess the safety profile of pharmaceutical products.
- Collaborating with cross-functional teams to ensure timely and accurate reporting of adverse events.
- Maintaining up-to-date knowledge of pharmacovigilance regulations and industry best practices to ensure compliance.
- Providing training and support to team members on pharmacovigilance reporting processes and requirements.
Your Profile:
You will bring relevant pharmacovigilance and drug safety experience, along with the following qualifications and skills.
Required qualifications and experience:
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Significant experience in pharmacovigilance reporting or drug safety within a clinical or pharmaceutical environment.
- Strong analytical skills with proficiency in data analysis tools and reporting software.
- Excellent communication and interpersonal skills, facilitating effective collaboration with internal and external stakeholders.
📌 Pharmacovigilance Specialist (Ciudad de México)
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📍 Ciudad de México
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