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.
Clinical Research Associate
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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 Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards âą Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution âą Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting âą Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct âą Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations
đŻ Requirements
âą Advanced degree in a relevant field such as life sciences, nursing, or medicine âą Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements âą Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills âą Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools âą Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment âą Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driverâs license
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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