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 Delivering clinical trial monitoring work to a high standard âą Coordinating all activities for setting up and monitoring a study âą Completing accurate study status reports and maintaining study documentation âą Running sponsor generated queries efficiently âą Participating in the preparation and review of study documentation and feasibility studies for new proposals as required âą Developing and maintaining strong, collaborative relationships with key stakeholders, clinical investigators, and site staff âą Ensuring patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements
âą University degree in medicine, science, or equivalent âą Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data âą Experience in Clinical Research as CTA or similar roles 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 60%)
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 March 24
Clinical Research Associate ensuring compliance with study protocols and ICH GCP regulations at clinical sites in Argentina. Primary responsibilities include data integrity and compliance oversight.
đŠđ· Argentina â Remote
đ° Venture Round on 1990-01
â° Full Time
đą Junior
đĄ Mid-level
đŹ Research Analyst