ICON plc
10,000+ employees
Founded 1990
đŒ Consulting
đ„ Healthcare
đŠ Logistics
Consulting âą Healthcare âą 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.
Clinical Data Coordinator
đ July 23
đ Check your resume score for this job
Improve your chances of getting an interview by checking your resume score before you apply.
ICON plc
10,000+ employees
Founded 1990
đŒ Consulting
đ„ Healthcare
đŠ Logistics
Consulting âą Healthcare âą 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.
đ Description
âą Deliver clinical data management work to a high standard, working closely with your team and stakeholders. âą Assist Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures. âą Manage clinical and third-party data reconciliation based on edit specifications and data review plans. âą Track and communicate status of study and task metrics to clinical data scientist, project team, and functional management. âą Address data related questions and recommend potential solutions. âą Identify root cause to systematically resolve data issues.
đŻ Requirements
âą Bachelor's degree in a relevant field, such as Life Sciences or Healthcare. âą Intermediate knowledge of clinical data management within the pharmaceutical or biotechnology industry. âą Familiarity with data management software and systems (e.g., Medidata, Oracle RDC, or similar). âą Strong attention to detail and the ability to work effectively in a fast-paced environment. âą Excellent communication skills and the ability to collaborate with cross-functional teams. âą Knowledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus.
đïž Benefits
âą Competitive base salary and performance related incentives âą Health and wellbeing programmes including medical, dental, and vision coverage where applicable âą Retirement and pension plans âą Life assurance and disability coverage âą Employee assistance programmes and wellbeing resources âą Learning and development opportunities through structured training and career pathways
Apply Now
