Clinical Data Programming Lead

🕒 July 22

🌐 Mexico, Chile, +3 more countries – Remote

🇲🇽 Mexico – Remote 🇨🇱 Chile – Remote 🇨🇴 Colombia – Remote 🇧🇷 Brazil – Remote 🇵🇪 Peru – Remote

⏰ Full Time

🟠 Senior

✨ Programming

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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

• Lead and oversee clinical data programming activities across multiple clinical trials, ensuring quality, timeliness, and regulatory compliance • Collaborate with cross-functional teams to develop programming strategies and standards for data collection, processing, and analysis • Provide technical expertise and guidance to programming team members, including best practices and troubleshooting support • Review and validate programming deliverables for accuracy, consistency, and adherence to predefined specifications • Contribute to innovative programming solutions that improve efficiency and data quality in clinical trials • Coordinate clinical data analysis delivery, resolve issues, and develop team capability • Travel as required, approximately 15%

🎯 Requirements

• Bachelor's degree or higher in Computer Science, Statistics, or a related field • Prior experience in clinical data programming within the pharmaceutical, biotechnology, or CRO industry • Proven leadership experience leading and mentoring programming professionals • Expertise in clinical research programming languages such as SAS, Python, and/or SQL • Strong understanding of CDISC standards, FDA/EMA regulations, and ICH-GCP guidelines • Ability to manage competing priorities and develop a team • Excellent communication, problem-solving, and decision-making skills • Willingness to travel as required, approximately 15% • 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 • Reasonable accommodations during the recruitment process • Inclusive and accessible workplace