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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

• Conduct remote review and analysis of clinical trial data to identify trends, anomalies, and potential risks to patient safety and data quality. • Collaborate with site personnel and clinical teams to address findings from centralized monitoring activities and implement corrective and preventive actions as necessary. • Utilize advanced data analytics tools and technology platforms to enhance the efficiency and effectiveness of centralized monitoring processes. • Provide support and guidance to study teams on centralized monitoring methodologies, best practices, and regulatory requirements. • Contribute to the development and optimization of centralized monitoring strategies and protocols to maximize data quality and compliance across clinical trials.

🎯 Requirements

• Bachelor's degree in life sciences, computer science, or a related discipline • Previous experience in clinical research, data management, or monitoring within the pharmaceutical, biotechnology, or CRO industry. • Strong understanding of clinical trial processes, regulations, and guidelines (e.g., ICH GCP, FDA regulations). • Excellent analytical and critical thinking skills with the ability to identify patterns, trends, and discrepancies in clinical trial data. • Effective communication and interpersonal skills, with the ability to collaborate cross-functionally and communicate complex concepts to diverse stakeholders. • Willingness to travel as required (approximately 5%)

🏖️ 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