Clinical Data Coordinator II

🕒 May 26

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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

• Coordinating data collection activities, ensuring accuracy and completeness of clinical trial data • Managing data entry processes and performing quality control checks to maintain data integrity • Collaborating with cross-functional teams, including clinical operations and data management, to address data-related issues and enhance project efficiency • Assisting in the development and implementation of data management plans and standard operating procedures • Staying current with industry trends and best practices in clinical data management to drive continuous improvement initiatives

🎯 Requirements

• Bachelor's degree in life sciences, data management, or a related field; advanced degree preferred • Proven experience in clinical data coordination or management within the clinical research industry • Strong analytical skills and attention to detail, with a focus on data accuracy and quality • Excellent communication and interpersonal skills, facilitating effective collaboration with diverse teams and stakeholders • Proficiency in data management systems and clinical trial management software • A commitment to maintaining high standards of quality and compliance in all data-related activities • Must be amenable to work homebased, midshift schedule (3pm-12mn PHT)

🏖️ 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