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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

• Foster relationships with clinical trial sites, enhancing site engagement, and contribute to the advancement of innovative treatments and therapies • Contribute to clinical research activities, taking responsibility for deliverables and working collaboratively • Build and maintain relationships with key stakeholders at clinical trial sites, including principal investigators, site coordinators, and research staff • Provide support and guidance to site staff on study protocols, procedures, and regulatory requirements • Identify opportunities to improve site engagement and optimize site performance through regular communication and feedback mechanisms • Collaborate with internal teams to develop and implement site engagement strategies tailored to the specific needs of each study and site • Monitor site performance metrics and provide regular updates to study teams on site engagement activities and outcomes

🎯 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, with the ability to build rapport and establish effective working relationships with diverse stakeholders • Excellent organizational and problem-solving skills, with the ability to prioritize and manage multiple tasks simultaneously • Knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials • Willingness to travel as required (approximately 60%)

🏖️ 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