Site Care Partner

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🕒 July 21

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ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

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

• Build and maintain strong relationships with principal investigators, site coordinators, and research staff at clinical trial sites • Provide support and guidance on study protocols, procedures, and regulatory requirements • Identify opportunities to improve site engagement and optimize site performance • Collaborate with internal teams to develop and implement tailored site engagement strategies • Monitor site performance metrics and provide regular updates to study teams on engagement activities and outcomes • Contribute to clinical research activities and take responsibility for deliverables

🎯 Requirements

• Bachelor's degree in life sciences or a related field • Previous experience in clinical research, site management, or a related field preferred • Strong interpersonal and communication skills • Excellent organizational and problem-solving skills • Ability to prioritize and manage multiple tasks simultaneously • Knowledge of ICH-GCP guidelines and clinical trial regulatory requirements • Willingness to travel as required, approximately 60% • Legal right to work in the country where the role is based

🏖️ 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