Senior Clinical Data Science Programmer

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ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💊 Pharmaceuticals

🧬 Biotechnology

⚕️ Healthcare Insurance

Pharmaceuticals • Biotechnology • Healthcare Insurance

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, validate, and maintain programming solutions for CDMS (EDC systems such as Rave/Veeva), data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials. • Collaborate with data managers, project managers, clinical data scientists, and biostatisticians to ensure the integration of programming solutions into the overall data management process. • Act as a primary point of contact during the study set up and maintenance phase for system programming related questions by the project team. • Support colleagues with the clinical trials environment and concepts of Clinical Data Management Systems. • Perform extracts of data from CDMS and creation of data transfer programs. • Act as mentor and provides guidance and support to more junior programmer levels assigned to a project. • Assist in the development and implementation of improvements to technical systems and processes within an SME role. • Provide guidance on programming best practices, coding standards, and data quality control measures. • Stay updated on advancements in programming languages and data management tools to enhance operational efficiencies.

🎯 Requirements

• Complete bachelor’s degree relevant field such as computer science, SAS, statistics, or life sciences. • Extensive experience in programming for CDMS (EDC systems such as Rave/Veeva), data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials with proficiency in languages such as SAS, R, or Python. • Strong problem-solving skills and the ability to work collaboratively in a fast-paced, cross-functional environment. • Excellent attention to detail and organizational skills, with a commitment to delivering high-quality results. • Strong communication and interpersonal skills, with the ability to effectively collaborate with diverse teams and influence outcomes. • MUST HAVE advanced English Communication, Writing and Reading

🏖️ 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