Senior Clinical Data Science Lead

🕒 August 18

🌐 Mexico, Colombia – Remote

🇲🇽 Mexico – Remote 🇨🇴 Colombia – Remote

⏰ Full Time

🟠 Senior

📊 Data Scientist

👻 Ghost score 33%

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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

• Develop and oversee timeliness of clinical data science activities during the life cycle of studies as it relates to data review and data delivery milestones • Provide input into clinical system development activities and clinical risk management activities • Track and keep functional management and those responsible for project management informed of issues affecting project target dates, scope, or budget • Escalate potential problems effectively and in a timely manner • Forecast budget, hours, and resourcing for clinical data review activities • Perform analytic review focusing on errors that matter or have a meaningful impact on subject safety or interpretation of the final analysis • Develop planning documents related to data review, data analytics, and data deliverables • Participate in Sponsor and/or third-party audits • Negotiate timelines and key deliverables with clients, external customers, vendors, and departments • Travel approximately 15% domestically and/or internationally

🎯 Requirements

• 5 + 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 as a functional lead of multiple low and moderately complex studies, whilst acting as a resource for less experienced colleagues • 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., Medidata Rave, Inform, Oracle Clinical, Veeva) • Excellent communication skills • Budget and timeline management experience • Data Analytic and Data Validation 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 • Applications must be submitted in English

🏖️ 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