Pharmacovigilance Associate

🕒 June 3

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ICON plc

WebsiteLinkedInAll Job Openings

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

• Collecting and reviewing adverse event reports to ensure accurate and timely reporting in accordance with regulatory guidelines. • Conducting signal detection and risk assessment activities to identify potential safety issues. • Collaborating with cross-functional teams to support safety-related inquiries and investigations. • Maintaining up-to-date knowledge of pharmacovigilance regulations and industry best practices. • Assisting in the preparation of safety reports and regulatory submissions.

🎯 Requirements

• Bachelor's degree in life sciences, pharmacy, or a related field; advanced degree preferred. • 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. • Must be amenable to work in midshift schedule (4pm-1am PHT) and in a homebased/remote setup

🏖️ 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