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.
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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 Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials âą Ensure protocol compliance, data integrity, and patient safety throughout the trial process âą Collaborate with investigators and site staff to facilitate smooth study conduct âą Perform data review and resolution of queries to maintain high-quality clinical data âą Contribute to the preparation and review of study documentation, including protocols and clinical study reports âą Play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to innovative treatments and therapies
âą Bachelor's degree in a scientific or healthcare-related field âą Minimum of 2 years of experience as a Clinical Research Associate âą In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines âą Strong organizational and communication skills, with attention to detail âą Ability to work independently and collaboratively in a fast-paced environment âą Ability to travel at least 60% of the time (international and domestic - fly and drive) âą Valid driver's license 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
Apply Nowđ August 10
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đČđœ Mexico â Remote
đ° Venture Round on 1990-01
â° Full Time
đĄ Mid-level
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đ§Ș Clinical Research
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đČđœ Mexico â Remote
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â° Full Time
đą Junior
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đ§Ș Clinical Research
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