Clinical Data Coordinator II
ICON PLC, Ladywell, West Lothian
Clinical Data Coordinator II
Salary not available. View on company website.
ICON PLC, Ladywell, West Lothian
- Full time
- Permanent
- Onsite working
Posted 5 days ago, 17 Sep | Get your application in now to be included in the first week's applications.
Closing date: Closing date not specified
Job ref: 087f7ad53d1645d1a9195cff38ea43aa
Location ref: Ladywell, West Lothian
Full Job Description
- Assist Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures.
- Manage clinical and third-party data reconciliation based on edit specifications and data review plans.
- Tracks and communicates status of study and task metrics to clinical data scientist, project team, and functional management.
- Address data related questions and recommend potential solutions.
- Identify root cause to systematically resolve data issues.
Bachelor's degree in a relevant field, such as Life Sciences or Healthcare. - Intermediate knowledge of clinical data management within the pharmaceutical or biotechnology industry.
- Familiarity with data management software and systems (e.g., Medidata, Oracle RDC, or similar).
- Strong attention to detail and the ability to work effectively in a fast-paced environment.
- Excellent communication skills and the ability to collaborate with cross-functional teams.
- Knowledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus.
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We're looking for a Clinical Data Coordinator II to join our growing team in Livingston, UK. This is a fantastic office based opportunity for recent graduates and early-career professionals who want to build hands-on experience in clinical research while working alongside experienced specialists in a collaborative, office-based environment. At ICON plc, you'll help support the design and analysis of clinical trials, work with real-world medical data, and develop valuable skills that contribute to the development of innovative new treatments. With strong mentorship and learning opportunities, this role offers an excellent starting point for building a career in the clinical research industry. - Various annual leave entitlements
- A range of health insurance offerings to suit you and your family's needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include:
Direct job link
https://www.s1jobs.com/job/clinical-data-coordinator-ii-127413481
About this company