10,000+ employees
Founded 1990
đ Pharmaceuticals
đ§Ź 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 3 days ago
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10,000+ employees
Founded 1990
đ Pharmaceuticals
đ§Ź 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.
âą Support the safety monitoring and reporting of pharmaceutical products âą Take responsibility for pharmacovigilance and drug safety deliverables, applying your skills to ensure quality and efficiency âą Support the collection, review, and processing of adverse event data in accordance with pharmacovigilance regulations and company procedures âą Assist in the preparation and submission of safety reports to regulatory authorities and stakeholders âą Collaborate with cross-functional teams to ensure timely and accurate communication of safety information âą Contribute to the development and maintenance of pharmacovigilance documentation, including standard operating procedures and safety management plans âą Participate in training and development activities to gain a deeper understanding of pharmacovigilance practices and regulatory requirements
âą Bachelor's degree in pharmacy, life sciences, or a related field âą Strong attention to detail and organizational skills, with the ability to manage multiple tasks and prioritize effectively âą Excellent communication and interpersonal skills, with the ability to work collaboratively in a team environment âą Basic understanding of pharmacovigilance principles and regulatory guidelines is desirable but not required; relevant training will be provided âą Proficiency in Microsoft Office applications, with good analytical and problem-solving skills âą Willingness to travel as required (approximately 10%)
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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