Graduate-level pharmacovigilance position supporting safety monitoring and adverse event reporting for pharmaceutical products. Role involves data processing, regulatory submissions, and cross-functional collaboration within a sponsor-dedicated model at a integral clinical research organization.
Responsibilities
Collect, review, and process adverse event data per pharmacovigilance regulations and procedures
Assist in preparing and submitting safety reports to regulatory authorities and stakeholders
Collaborate with cross-functional teams on safety information communication
Contribute to pharmacovigilance documentation including SOPs and safety management plans
Participate in training to develop expertise in pharmacovigilance practices and regulations
Requirements
Bachelor's degree in pharmacy, life sciences, or related field
Strong attention to detail and organizational skills with multitasking ability
Excellent written and verbal communication skills
Proficiency in Microsoft Office applications
Analytical and problem-solving capabilities
Willingness to travel approximately 10% as required

📌 Graduate Pharmacovigilance Associate (Xico)
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📍 Xico