Site Management Associate, Greek

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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

• Coordinate monitoring activities at clinical trial sites, ensuring adherence to study protocols and timely resolution of site-related issues • Assist in preparing and reviewing regulatory documents and ensure site activities comply with GCP and applicable regulations • Collaborate with cross-functional teams to support trial sites throughout the study lifecycle • Track site performance metrics, analyze data, and provide reports to improve site management efficiency • Participate in training initiatives and mentor junior staff to support their development in clinical trial management

🎯 Requirements

• Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research • Fluent in English and Greek, with excellent written and verbal communication skills • Experience in clinical research, site management, or monitoring • Solid understanding of clinical trial processes and Good Clinical Practice (GCP) guidelines • Strong organizational and project management skills • Ability to handle multiple priorities and deadlines • Excellent analytical skills and attention to detail • Focus on maintaining high-quality standards • Exceptional communication and interpersonal skills • Ability to build and maintain effective relationships with site personnel and cross-functional teams • Willingness to travel as required, approximately 25% • 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 • Inclusion and accessibility support, including reasonable accommodations during the recruitment process