Pharmacovigilance Supervisor

🔥 0 minutes ago

🇲🇽 Mexico – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

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ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

📋 Description

• Oversee the safety monitoring and reporting of adverse events related to clinical trials and marketed products. • Manage day-to-day pharmacovigilance and drug safety activities. • Supervise pharmacovigilance operations, ensuring timely and accurate reporting of adverse events. • Collaborate with clinical operations and regulatory affairs to optimize pharmacovigilance processes. • Ensure compliance with global regulatory requirements and internal standard operating procedures for safety reporting. • Manage safety data collection, analysis, and submission to regulatory authorities. • Provide leadership and training to the pharmacovigilance team.

🎯 Requirements

• Bachelor's degree in life sciences, pharmacy, or a related field. • Experience in pharmacovigilance or drug safety, with a focus on clinical trials or post-marketing surveillance. • Strong knowledge of global pharmacovigilance regulations and guidelines. • Excellent communication, leadership, and organizational skills, with the ability to manage a team effectively. • Detail-oriented with the ability to manage multiple tasks and ensure accuracy in safety reporting. • Legal right to work in the country where the role is based.

🏖️ Benefits

• Competitive base salary and performance related incentives • Health and wellbeing programmes including medical, dental, and vision coverage where applicable • Retirement and pension plans • Life assurance and disability coverage • Employee assistance programmes and wellbeing resources • Learning and development opportunities through structured training and career pathways

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