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.
🕒 May 26
Improve your chances of getting an interview by checking your resume score before you apply.
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.
• Take responsibility for clinical trial monitoring deliverables, ensuring quality and efficiency • Assist in the planning, initiation, and execution of clinical trial activities • Conduct site feasibility assessments and participate in site selection processes • Coordinate with investigative sites to ensure compliance with study protocols and regulatory requirements • Monitor study progress and data collection activities to ensure quality and accuracy • Assist in the preparation and review of study documentation and reports
• Bachelor's degree in a relevant field, such as life sciences or healthcare • 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 Now🕒 May 26
Data and Documentation Technician managing customer requests and documentation quality at IFF. Ensuring compliance with standards and supporting global market initiatives.
🕒 April 15
Dairy Performance Support professional enhancing customer success through technical training and automation solutions in the LATAM region. Join a global leader in innovative dairy technology.
🗣️🇧🇷🇵🇹 Portuguese Required