ICON plc
10,000+ employees
Founded 1990
đ Pharmaceuticals
𧏠Biotechnology
âïž Healthcare Insurance
Pharmaceuticals âą Biotechnology âą 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.
Pharmacovigilance Supervisor
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đ„ 54 minutes ago
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ICON plc
10,000+ employees
Founded 1990
đ Pharmaceuticals
𧏠Biotechnology
âïž Healthcare Insurance
Pharmaceuticals âą Biotechnology âą 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.
đ Description
âą Manage day-to-day pharmacovigilance and drug safety activities, supporting your team to deliver quality outcomes âą Supervising the day-to-day pharmacovigilance operations, ensuring timely and accurate reporting of adverse events âą Collaborating with cross-functional teams, including clinical operations and regulatory affairs, to optimize pharmacovigilance processes âą Ensuring compliance with global regulatory requirements and internal standard operating procedures for safety reporting âą Managing safety data collection, analysis, and submission to regulatory authorities âą Providing leadership and training to the pharmacovigilance team, ensuring adherence to best practices in safety monitoring
đŻ Requirements
âą Bachelor's degree in life sciences, pharmacy, or a related field âą Experience in pharmacovigilance or drug safety, with a focus on clinical trials or post-marketing surveillance âą Strong knowledge of global pharmacovigilance regulations and guidelines âą Excellent communication, leadership, and organizational skills, with the ability to manage a team effectively âą Detail-oriented with the ability to manage multiple tasks and ensure accuracy in safety reporting.
đïž Benefits
âą Competitive base salary and performance related incentives âą Health and wellbeing programmes including medical, dental, and vision coverage where applicable âą Retirement and pension plans âą Life assurance and disability coverage âą Employee assistance programmes and wellbeing resources âą Learning and development opportunities through structured training and career pathways
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