10,000+ employees
Founded 1990
đŒ Consulting
đ„ Healthcare
đŠ Logistics
Consulting âą Healthcare âą Logistics
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„ 10 hours ago
Where this job comes from
Posted on ICON plc's careers page, not through a job board
First seen by Remote Rocketship 10 hours ago
Still open on ICON plc's site. Checked 1 hour ago.
10,000+ employees
Founded 1990
đŒ Consulting
đ„ Healthcare
đŠ Logistics
Consulting âą Healthcare âą Logistics
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 Deliver clinical trial monitoring work to a high standard âą Coordinate all activities for setting up and monitoring a study âą Complete accurate study status reports and maintain study documentation âą Run sponsor-generated queries efficiently and take responsibility for study cost efficiency âą Participate in the preparation and review of study documentation and feasibility studies for new proposals as required âą Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff âą Ensure patient safety and compliance with ICON's procedures, protocols, and regulatory requirements
âą University degree in medicine, science âą Pathology lab experience âą Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data âą Excellent written and verbal communication in English âą Good social skills enabling you to deal with queries in a timely manner âą Willingness to travel as required (approximately 30%) âą Legal right to work in the country where the role is based
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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