10,000+ employees
Founded 1990
đ Pharmaceuticals
đ§Ź Biotechnology
âïž Healthcare Insurance
Pharmaceuticals âą Biotechnology âą 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.
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10,000+ employees
Founded 1990
đ Pharmaceuticals
đ§Ź Biotechnology
âïž Healthcare Insurance
Pharmaceuticals âą Biotechnology âą 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.
âą Designing and implementing clinical trial protocols, ensuring adherence to scientific and regulatory standards âą Conducting data analysis and interpretation to derive insights that support study objectives âą Collaborating with cross-functional teams to ensure effective study execution and data quality âą Engaging with stakeholders to communicate findings and contribute to scientific discussions âą Assisting in the preparation of regulatory submissions, study reports, and scientific publications
âą Bachelor's degree in a relevant scientific discipline or healthcare-related field âą Experience in clinical research or a related scientific role, with a strong understanding of clinical trial processes âą Excellent analytical skills and proficiency in data interpretation and statistical analysis âą Strong communication and collaboration skills, with the ability to work effectively in interdisciplinary teams âą Detail-oriented and committed to maintaining high standards of data integrity and quality âą Willingness to travel as required (approximately 20%)
âą Competitive base salary and performance related incentives âą Health and wellbeing programmes including medical, dental, and vision coverage where applicable âą Retirement and pension plans âą Life assurance and disability coverage âą Employee assistance programmes and wellbeing resources âą Learning and development opportunities through structured training and career pathways
Apply Nowđ„ 11 hours ago
51 - 200
đ§Ź Biotechnology
đ Pharmaceuticals
âïž Healthcare Insurance
Senior Biostatistician performing statistical analyses to support clinical trial submissions at Cytel. Collaborating on protocol development and preparing clinical study reports for regulatory agencies.