Senior Manager, Pharmacovigilance

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🕒 June 30

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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 pharmacovigilance and drug safety operations, balancing quality, timelines, and stakeholder expectations • Manage the pharmacovigilance team to ensure timely and accurate reporting of adverse events and safety data in compliance with regulatory standards • Develop and implement pharmacovigilance policies and procedures to enhance safety monitoring and risk management practices • Collaborate with cross-functional teams, including clinical operations and regulatory affairs, to ensure integration of safety data into clinical development plans • Monitor and analyze safety data trends to identify potential risks and inform decision-making for ongoing clinical trials • Stay updated on industry regulations and best practices in pharmacovigilance to drive continuous improvement initiatives

🎯 Requirements

• Bachelor's degree in a relevant scientific discipline or healthcare-related field • Significant experience in pharmacovigilance or drug safety, ideally within the clinical research or pharmaceutical industries • Strong understanding of regulatory requirements related to drug safety and reporting • Excellent analytical and problem-solving skills, with a focus on data-driven decision-making • Strong communication and interpersonal skills, capable of engaging and influencing diverse stakeholders

🏖️ 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