Pharmacovigilance Associate

🕒 June 11

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Logo of ICON plc

ICON plc

10,000+ employees

Founded 1990

💊 Pharmaceuticals

🧬 Biotechnology

⚕️ Healthcare Insurance

Pharmaceuticals • Biotechnology • Healthcare Insurance

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

• Monitor and ensure the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information • Deliver pharmacovigilance and drug safety work to a high standard, working closely with your team and stakeholders • Collect and review adverse event reports to ensure accurate and timely reporting in accordance with regulatory guidelines • Conduct signal detection and risk assessment activities to identify potential safety issues • Collaborate with cross-functional teams to support safety-related inquiries and investigations • Maintain up-to-date knowledge of pharmacovigilance regulations and industry best practices • Assist in the preparation of safety reports and regulatory submissions

🎯 Requirements

• Bachelor's degree in a relevant scientific discipline or healthcare-related field • Experience in pharmacovigilance, drug safety, or a related area, preferably within a clinical or pharmaceutical environment • Strong analytical skills with attention to detail in data collection and reporting • Excellent communication and interpersonal skills, enabling effective collaboration with team members and stakeholders • A commitment to maintaining high standards of quality and compliance in all pharmacovigilance activities • Willingness to travel as required (approximately 10%)

🏖️ 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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