Clinical Trial Designer

Job not on LinkedIn

🔥 0 minutes ago

🔔 Pennsylvania – Remote

🔔 Pennsylvania – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

✍️ Designer

👻 Ghost score 10%

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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 systems and applications to enhance data collection and management processes • Collaborate with cross-functional teams to gather requirements and translate them into system specifications • Conduct system testing and validation to ensure compliance with regulatory requirements and user needs • Provide training and support to users, addressing issues during system usage • Participate in continuous improvement of clinical systems by incorporating user feedback and industry best practices • Take responsibility for creative design and content deliverables, ensuring quality and efficiency

🎯 Requirements

• Degree in computer science, information technology, life sciences, or a related field • Experience in system design and implementation, preferably within a clinical research environment • Strong understanding of clinical trial processes and regulatory requirements • Excellent problem-solving skills and attention to detail in system functionality and usability • Effective communication and collaboration skills, with the ability to work well in cross-functional teams • Willingness to travel as required (approximately 10%) • 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