Clinical Data Manager – II

🔥 3 hours ago

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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

• You will oversee clinical data science workstreams, ensuring deliverables meet quality and timeline expectations • Leading the development and implementation of clinical data management strategies to optimize data collection, analysis, and reporting • Collaborating with cross-functional teams to ensure the accurate integration of data science techniques into clinical trial designs • Overseeing the analysis of clinical data to provide actionable insights that inform study decisions and outcomes • Providing strategic guidance on data governance, quality control, and compliance with regulatory requirements • Establishing partnerships with key stakeholders to leverage the latest advancements in data science and technology in clinical research

🎯 Requirements

• Bachelor's degree in Life Sciences, Computer Science, or a related field • 8 to 10 years of clinical data management experience, including Early Development and Phase I studies • Experience leading at least three study start ups and three database locks • Strong knowledge of clinical data management, data review, and data quality processes • Experience participating in User Acceptance Testing and reviewing data reports • Comfortable managing frequent real time data extractions and supporting rapid study decisions • Experience leading post production changes and change control activities • Experience overseeing Clinical Data Coordinators and delegated activities • Experience managing external data vendors and third party data deliverables • Exposure to dose escalation studies and meetings preferred • Strong leadership skills with experience working across cross functional teams • Proficient in data analysis tools, statistical software, and data visualization • Excellent communication, stakeholder management, and problem solving skills • Proactive approach with the confidence to research, resolve issues, and drive outcomes • CRO oversight experience preferred but not required • Willingness to travel up to 15 percent as required

🏖️ 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