Clinical Data Coordinator

**Clinical Data Coordinator****JR ****Site: Mexico**At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organization: Accountability & Delivery, Collaboration, Partnership, and Integrity. We want to be the Clinical Research Organization that delivers excellence to our clients and to patients at every touchpoint. In short, to be the partner of choice in drug development.That’s our vision. We’re driven by it. And we need talented people who share it.If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.**Overview**:Supports and executes the data review activities, including data validation and analytics, that contribute to delivery of clinical data that meets agreed upon data integrity standards**The role**:- Performs duties at a high standard of quality under general supervision.- Maintains clinical data management related study documentation as appropriate.- Manages third party data reconciliation and data review process.- Trains other team members in clinical data management skills and processes for individual studies.- Utilizes internal systems to optimize and communicate resourcing issues and needs.- Ensures study and task metrics are tracked and communicated to the clinical data scientist, project team and functional management- Addresses data related questions and recommends potential solutions; escalates issues that potentially impact study analysis.- Documents data issues within system of record for communication of issues with owners. Identifies root cause to systematically resolve data issues.- Responsible for review of standard quality indicator review including root cause analysis for identification of underlying causes of outliers and trend analysis.- May support or provide input into clinical system development activities including data lake mapping.- May be responsible for local lab normal range data entry activities and identification and documentation of data problems during lab normal range tracking.- May participate in sponsor and/or third(1)party audits.**You will need**:- Intermediate knowledge of clinical data management- Basic knowledge of the drug development process including risk based monitoring principles- Working knowledge and understanding of clinical data management systems or electronic data capture software1 year of relevant experienceBachelor’s degree in relevant field of studyAdvanced English to Read, write, and speak**Benefits of Working in ICON**:Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.LI-FB1