ICON seeks a graduate-level pharmacovigilance associate to support drug safety monitoring and regulatory reporting activities. The home-based role in Mexico City involves adverse event processing, safety documentation, and cross-functional collaboration within a integral clinical research organization.
Responsibilities
Support collection, review, and processing of adverse event data per regulations
Assist in preparing and submitting safety reports to regulatory authorities
Collaborate with cross-functional teams on safety information communication
Contribute to development and maintenance of pharmacovigilance documentation
Participate in training activities to build pharmacovigilance expertise
Requirements
Bachelor's degree in pharmacy, life sciences, or related field
Strong attention to detail and organizational skills with multitasking ability
Excellent communication and interpersonal skills for team collaboration
Proficiency in Microsoft Office applications
Analytical and problem-solving skills
Willingness to travel approximately 10% as required

📌 Graduate Pharmacovigilance Associate (Xico)
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📍 Xico