10,000+ employees
Founded 1990
đź’Š 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.
đź•’ 2 days ago
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10,000+ employees
Founded 1990
đź’Š 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.
• Support clinical trial deliverables, applying your skills to ensure quality and efficiency • Independently support the planning, execution, and reporting of clinical trials across all phases and therapeutic areas • Maintain and analyze trial tracking systems, ensuring data accuracy and compliance • Track and analyze trial budgets, including actual vs. planned spend, and follow up on variances • Manage the Trial Master File (TMF), ensuring completeness and inspection readiness • Oversee investigational product (IP) and ancillary supply management, including ordering, distribution, and tracking • Coordinate site and country feasibility assessments and regulatory documentation processes • Prepare and analyze key clinical trial data reports and metrics
• Bachelor's degree in a relevant field, such as life sciences or healthcare preferred • Previous experience in clinical research or a related field preferred • Strong organizational and communication skills • Ability to work independently and collaboratively in a fast-paced environment • Attention to detail and ability to prioritize tasks effectively
• 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
Apply Nowđź•’ 2 days ago
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