Clinical Scientist

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🌐 Mexico, Colombia, +1 more countries – Remote

🇲🇽 Mexico – Remote 🇨🇴 Colombia – Remote 🇧🇷 Brazil – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

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ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • 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.

📋 Description

• Design and implement clinical trial protocols, ensuring adherence to scientific and regulatory standards • Conduct data analysis and interpretation to derive insights supporting study objectives • Collaborate with cross-functional teams to ensure effective study execution and data quality • Engage with stakeholders to communicate findings and contribute to scientific discussions • Assist in preparing regulatory submissions, study reports, and scientific publications • Take responsibility for clinical research deliverables, applying skills to ensure quality and efficiency

🎯 Requirements

• Bachelor's degree in a relevant scientific discipline or healthcare-related field • Experience in clinical research or a related scientific role • Strong understanding of clinical trial processes • Excellent analytical skills • Proficiency in data interpretation and statistical analysis • Strong communication and collaboration skills • Ability to work effectively in interdisciplinary teams • Detail-oriented and committed to maintaining high standards of data integrity and quality • Willingness to travel as required, approximately 20% • Legal right to work in the country where the role is based

🏖️ Benefits

• Competitive base salary and performance related incentives • Health and wellbeing programmes including medical, dental, and vision coverage where applicable • Retirement and pension plans • Life assurance and disability coverage • Employee assistance programmes and wellbeing resources • Learning and development opportunities through structured training and career pathways