Clinical Data Coordinator II
PRA Health Sciences
Req #: 111739
Type: Argentina
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Overview: As a Clinical Data Coordinator you will play a key role in improving the lives of patients by accelerating the development of our customers drugs and devices through innovative solutions. You will play a vital client facing line management role, embedded in our clients business. You will be responsible for the management of day to day biostatistics activities, ensuring everyone is well-trained on ICON standard processes, and promoting efficiency, quality, and timeliness in project work Responsibilities: What you will be doing: A Clinical Data Coordinator (CDC I) is a professional in Data Management who performs data review and cleaning tasks to achieve a high quality clinical database. Is an integral part of the overall project team and completes tasks to meet data management project goals and deadlines to reach a final high quality clinical database for analysis. * Supports activities related to development of the clinical data management systems (CDMS), as needed. * Supports and executes the data review activities, including data validation and analytics, associated with a clinical trial to ensure the end product of clinical data meets agreed upon data integrity standards. * Maintains clinical data management related study documentation as appropriate. * Ensures study and task metrics are tracked and communicated to the clinical data scientist, project team and functional management. Qualifications: You are: * Bachelor's degree in Science or Health * Previus experience in Clinical Trial / Data management is a plus * Advanced English * Based in Buenos Aires - 100% remote Why ICON? Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future. Our success depends on the knowledge, capabilities and quality of our people. That's why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development. ICON, including subsidiaries, 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, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
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