Senior Clinical Trial Associate

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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

• Provide administrative support for clinical trials, including managing documentation, coordinating meetings, and maintaining trial-related records • Assist in the preparation and submission of regulatory documents and ensuring compliance with study protocols and regulatory requirements • Collaborate with cross-functional teams to support trial operations and resolve any issues that arise during the course of the study • Monitor and track trial progress, including managing site communications and ensuring timely delivery of study materials • Build and maintain strong relationships with site staff and other stakeholders to facilitate smooth trial operations and support overall project success

🎯 Requirements

• Bachelor's degree in a relevant scientific discipline or healthcare-related field • Extensive experience in a clinical trial support role, with a solid understanding of clinical trial processes and regulatory requirements • Strong organizational and multitasking skills, with the ability to manage multiple tasks and projects effectively • Proficiency in clinical trial management systems and relevant software, with a keen eye for detail in documentation and data management • Excellent communication, interpersonal, and problem-solving skills, with the ability to work collaboratively with diverse teams and stakeholders • 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