CDC I

As a Clinical Data Coordinator I at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. Your responsibilities will include: - Assisting Data Management Study Lead in the development of eCRF, Data Validation Specifications, and Study Specific Procedures. - Reviewing clinical and third-party data based on edit specifications and data review plans. - Issuing clear, accurate, and concise queries to investigational sites. - Communicating effectively with peers, clinical data scientists, and functional management as required. - Performing other project activities as needed to ensure study timelines are met, such as filing and archiving study documentation and dispatching queries to investigator sites for resolution. Your profile should ideally include: - Bachelor's degree in a relevant field, such as Life Sciences or Healthcare. - Basic knowledge of clinical data management within the pharmaceutical or biotechnology industry. - Familiarity with data management software and systems like 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 like ICH-GCP is a plus. ICON offers a range of benefits designed to support your well-being and work-life balance, such as various annual leave entitlements, health insurance options, retirement planning offerings, a Global Employee Assistance Programme, life assurance, and more. The company values a diverse culture that rewards high performance and nurtures talent. If you are interested in the role, ICON encourages you to apply regardless of meeting all requirements, as you may be the perfect fit for the position or other roles within the organization.,