Principal Clinical Data Science Lead

🔥 23 hours ago

🌐 Colombia, Mexico, +1 more countries – Remote

🇨🇴 Colombia – Remote 🇲🇽 Mexico – Remote 🇺🇸 United States – Remote

⏰ Full Time

🟠 Senior

📊 Data Scientist

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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 serve as the primary contact for end-to-end data review activities performed on clinical trials • Ensure clinical data science deliverables are completed on time, with high quality, and within agreed financial metrics • Serve as the primary point of contact for internal and external team members regarding clinical data review activities • Lead data review activities to ensure delivery of data fit for analysis • Provide input into clinical system development and clinical risk management activities • Develop and oversee the timeliness of clinical data science activities throughout study lifecycles • Participate in sponsor and/or third-party audits • Forecast budget, hours, and resourcing for clinical data review activities • Perform analytic review focused on errors affecting subject safety or interpretation of final analysis • Develop planning documents related to data review, data analytics, and data deliverables • Establish approaches and lead resources to achieve operational and strategic plans • Travel approximately 15% domestically and/or internationally

🎯 Requirements

• 8+ years of clinical data management experience in a clinical research organization or pharmaceutical company • 2+ years of experience working in a clinical research organization (CRO) • Experience with all steps within the data science lifecycle and most major data science study tasks • Proficiency in at least one Clinical Data Management system required (e.g., Rave, Inform, Oracle Clinical, OCRDC, UX EDC) • Strong project management skills with experience leading multiple projects simultaneously • Excellent leadership and communication skills • Budget and timeline management experience • Data Analytic and Data Validation experience • Established Mentor and/or SME experience • Bachelor’s degree or local equivalent • Equivalent combination of education, training, and relevant experience may be considered in place of the education and experience stated above • All employees must read, write, and speak fluent English and host country language • 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