Lead Clinical Data Manager

🔥 1 hour ago

🔔 Pennsylvania – Remote

🔔 Pennsylvania – 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 oversee the planning, execution, and delivery of clinical data management activities for assigned projects • Collaborate with cross-functional teams to develop data management plans and ensure adherence to regulatory requirements and industry standards • Provide leadership and guidance to data management team members throughout the lifecycle of clinical trials • Perform data review and reconciliation activities to ensure accuracy, completeness, and consistency of clinical data • Contribute to the development and implementation of data management processes and best practices to optimize efficiency and quality

🎯 Requirements

• Bachelor's degree or higher in a relevant scientific discipline • Minimum of 4-5 years of experience in clinical data management within the pharmaceutical, biotechnology, or CRO industry • Proficiency in CDISC standards, FDA/EMA regulations, and ICH-GCP guidelines • Strong technical skills with experience in EDC systems and data management tools (e.g., Rave, Inform, Medidata) • Excellent communication, leadership, and problem-solving skills with the ability to work effectively in a team environment and manage multiple priorities simultaneously • Willingness to travel as required (approximately 10%)

🏖️ 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