ICON plc
10,000+ employees
Founded 1990
đ Pharmaceuticals
𧏠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.
Medical Director
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ICON plc
10,000+ employees
Founded 1990
đ Pharmaceuticals
𧏠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.
đ Description
âą Providing medical and scientific oversight for clinical trials, ensuring the safety of subjects and the integrity of trial data. âą Collaborating with clinical operations, regulatory, and safety teams to drive the successful execution of early phase clinical studies. âą Developing and reviewing clinical study protocols, study reports, and other key study documents. âą Interpreting clinical trial data and providing medical insights to inform decision-making and guide clinical development strategies.
đŻ Requirements
âą Medical degree (MD) or (DO) âą Extensive experience in clinical research and development, ideally as a Principal Investigator for Early Phase clinical trials âą Clinical Practice Experience, ideally in general medicine. âą Advanced English proficiency âą Medical Monitoring experience highly preferred âą Strong understanding of clinical trial design, regulatory requirements, and GCP guidelines. âą Exceptional analytical and problem-solving skills, with a focus on interpreting clinical data and driving evidence-based decisions. âą Excellent leadership, communication, and collaboration skills, with the ability to work effectively in cross-functional, global teams.
đïž Benefits
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
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